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Volumn 30, Issue , 1996, Pages 173-195

Parental imprinting and human disease

Author keywords

allelic methylation and replication; Angelman syndrome; Beckwith Wiedemann syndrome; Prader Willi syndrome; Wilms' tumor

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11P; CHROMOSOME 15Q; DNA METHYLATION; DNA REPLICATION; GENE LOCUS; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HEMIZYGOSITY; HUMAN; NEPHROBLASTOMA; PARENT; PRADER WILLI SYNDROME; PRIORITY JOURNAL; REVIEW; UNIPARENTAL DISOMY;

EID: 0030458551     PISSN: 00664197     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.genet.30.1.173     Document Type: Review
Times cited : (138)

References (174)
  • 1
    • 84995191751 scopus 로고
    • "Puppet" children: A report on three cases
    • Angelman H. 1965. "Puppet" children: a report on three cases. Dev. Med. Child. Neurol. 7:681-88
    • (1965) Dev. Med. Child. Neurol. , vol.7 , pp. 681-688
    • Angelman, H.1
  • 2
    • 0027426276 scopus 로고
    • Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14
    • Antonarakis SE, Blouin JL, Maher J, Avramopoulos D, Thomas G, Talbot CC. 1993. Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14. Am. J. Hum. Genet. 52:1145-52
    • (1993) Am. J. Hum. Genet. , vol.52 , pp. 1145-1152
    • Antonarakis, S.E.1    Blouin, J.L.2    Maher, J.3    Avramopoulos, D.4    Thomas, G.5    Talbot, C.C.6
  • 3
    • 0027280881 scopus 로고
    • Methylation and imprinting: From host defense to gene regulation?
    • Barlow DP. 1993. Methylation and imprinting: from host defense to gene regulation? Science 260:309-10
    • (1993) Science , vol.260 , pp. 309-310
    • Barlow, D.P.1
  • 4
    • 0029587022 scopus 로고
    • Gametic imprinting in mammals
    • Barlow DP. 1995. Gametic imprinting in mammals. Science 270:1610-13
    • (1995) Science , vol.270 , pp. 1610-1613
    • Barlow, D.P.1
  • 5
    • 0026098090 scopus 로고
    • The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
    • Barlow DP, Stoger R, Herrmann BG, Saito K, Schweifer N. 1991. The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature 349:84-87
    • (1991) Nature , vol.349 , pp. 84-87
    • Barlow, D.P.1    Stoger, R.2    Herrmann, B.G.3    Saito, K.4    Schweifer, N.5
  • 6
    • 0027203606 scopus 로고
    • Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
    • Bartolomei MS, Webber AL, Brunkow ME, Tilghman SM. 1993. Epigenetic mechanisms underlying the imprinting of the mouse H19 gene. Genes Dev. 7:1663-73
    • (1993) Genes Dev. , vol.7 , pp. 1663-1673
    • Bartolomei, M.S.1    Webber, A.L.2    Brunkow, M.E.3    Tilghman, S.M.4
  • 7
    • 0025809321 scopus 로고
    • Parental imprinting of the mouse H19 gene
    • Bartolomei MS, Zemel S, Tilghman SM. 1991. Parental imprinting of the mouse H19 gene. Nature 351:153-55
    • (1991) Nature , vol.351 , pp. 153-155
    • Bartolomei, M.S.1    Zemel, S.2    Tilghman, S.M.3
  • 8
    • 0000077851 scopus 로고
    • Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly
    • Beckwith JB. 1969. Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly. Birth Defects 5:188-90
    • (1969) Birth Defects , vol.5 , pp. 188-190
    • Beckwith, J.B.1
  • 9
    • 0029089444 scopus 로고
    • Factors affecting the timing and imprinting of replication on a mammalian chromosome
    • Bickmore WA, Carothers AD. 1995. Factors affecting the timing and imprinting of replication on a mammalian chromosome. J. Cell Sci. 108:2801-9
    • (1995) J. Cell Sci. , vol.108 , pp. 2801-2809
    • Bickmore, W.A.1    Carothers, A.D.2
  • 10
    • 0028920403 scopus 로고
    • Single cell analysis demonstrating somatic mosaicism involving lip in a patient with paternal isodisomy and Beckwith-Wiedemann syndrome
    • Bischoff FZ, Feldman GL, McCaskill C, Subramanian S, Hughes MR, Shaffer LG. 1995. Single cell analysis demonstrating somatic mosaicism involving lip in a patient with paternal isodisomy and Beckwith-Wiedemann syndrome. Hum. Mol. Genet. 4:395-99
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 395-399
    • Bischoff, F.Z.1    Feldman, G.L.2    McCaskill, C.3    Subramanian, S.4    Hughes, M.R.5    Shaffer, L.G.6
  • 12
    • 0028939902 scopus 로고
    • Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
    • Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, et al. 1995. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat. Genet. 9:395-400
    • (1995) Nat. Genet. , vol.9 , pp. 395-400
    • Buiting, K.1    Saitoh, S.2    Gross, S.3    Dittrich, B.4    Schwartz, S.5
  • 13
    • 0029868661 scopus 로고    scopus 로고
    • Familial cryptic translocation resulting in Angelman Syndrome: Implications for imprinting or location of the Angleman gene?
    • Burke LW, Wiley JE, Glenn CC, Driscoll DJ, Loud KM, et al. 1996. Familial cryptic translocation resulting in Angelman Syndrome: implications for imprinting or location of the Angleman gene? Am. J. Hum. Genet. 58:777-84
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 777-784
    • Burke, L.W.1    Wiley, J.E.2    Glenn, C.C.3    Driscoll, D.J.4    Loud, K.M.5
  • 14
    • 0025181455 scopus 로고
    • Prader-Willi syndrome, current understanding of cause and diagnosis
    • Butler MG. 1990. Prader-Willi syndrome, current understanding of cause and diagnosis. Am. J. Med. Genet. 35:319-32
    • (1990) Am. J. Med. Genet. , vol.35 , pp. 319-332
    • Butler, M.G.1
  • 15
    • 0022462350 scopus 로고
    • Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
    • Butler MG, Meaney FJ, Palmer CG. 1986. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome. Am. J. Med. Genet. 23:793-809
    • (1986) Am. J. Med. Genet. , vol.23 , pp. 793-809
    • Butler, M.G.1    Meaney, F.J.2    Palmer, C.G.3
  • 16
    • 0021094659 scopus 로고
    • Parental origin of chromosome 15 deletion in Prader-Willi syndrome
    • Butler MG, Palmer CG. 1983. Parental origin of chromosome 15 deletion in Prader-Willi syndrome. Lancet 1:1285-86
    • (1983) Lancet , vol.1 , pp. 1285-1286
    • Butler, M.G.1    Palmer, C.G.2
  • 17
    • 0028926888 scopus 로고
    • Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: One probably imprinted, another associated with N-myc amplification
    • Caron H, Peter M, van Sluis P, Speleman F, de Kraker J, et al. 1995. Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification. Hum. Mol. Genet. 4:535-39
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 535-539
    • Caron, H.1    Peter, M.2    Van Sluis, P.3    Speleman, F.4    De Kraker, J.5
  • 18
    • 84970049889 scopus 로고
    • Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification
    • Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, et al. 1993. Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification. Nat. Genet. 4:187-90
    • (1993) Nat. Genet. , vol.4 , pp. 187-190
    • Caron, H.1    Van Sluis, P.2    Van Hoeve, M.3    De Kraker, J.4    Bras, J.5
  • 19
    • 0027017879 scopus 로고
    • A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
    • Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, et al. 1992. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nat. Genet. 2:270-74
    • (1992) Nat. Genet. , vol.2 , pp. 270-274
    • Cattanach, B.M.1    Barr, J.A.2    Evans, E.P.3    Burtenshaw, M.4    Beechey, C.V.5
  • 20
    • 0028108657 scopus 로고
    • Genetic imprinting in the mouse:implications for gene regulation
    • Cattanach BM, Jones J. 1994. Genetic imprinting in the mouse:implications for gene regulation. J. Inherit Metab. Dis. 17:403-20
    • (1994) J. Inherit Metab. Dis. , vol.17 , pp. 403-420
    • Cattanach, B.M.1    Jones, J.2
  • 21
    • 0026248022 scopus 로고
    • The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7
    • Chaillet JR, Knoll JH, Horsthemke B, Lalande M. 1991. The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7. Genomics 11:73-776
    • (1991) Genomics , vol.11 , pp. 73-776
    • Chaillet, J.R.1    Knoll, J.H.2    Horsthemke, B.3    Lalande, M.4
  • 24
    • 0027280613 scopus 로고
    • Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas
    • Cheng JM, Hiemstra JL, Schneider SS, Naumova A, Cheung NKV, et al. 1993. Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas. Nat. Genet. 4:191-94
    • (1993) Nat. Genet. , vol.4 , pp. 191-194
    • Cheng, J.M.1    Hiemstra, J.L.2    Schneider, S.S.3    Naumova, A.4    Cheung, N.K.V.5
  • 25
    • 0029011991 scopus 로고
    • Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients
    • Christian SL, Robinson WP, Huang B, Mutirangura A, Line MR, et al. 1995. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients. Am. J. Hum. Genet. 57:40-48
    • (1995) Am. J. Hum. Genet. , vol.57 , pp. 40-48
    • Christian, S.L.1    Robinson, W.P.2    Huang, B.3    Mutirangura, A.4    Line, M.R.5
  • 27
    • 0028301177 scopus 로고
    • Developmental regulation of genomic imprinting of the IGF2 gene in human liver
    • Davies SM. 1994. Developmental regulation of genomic imprinting of the IGF2 gene in human liver. Cancer Res. 54:2560-62
    • (1994) Cancer Res. , vol.54 , pp. 2560-2562
    • Davies, S.M.1
  • 28
    • 0025320906 scopus 로고
    • A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting
    • DeChiara TM, Estratiadis A, Robertson EJ. 1990. A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 345:88-80
    • (1990) Nature , vol.345 , pp. 88-180
    • Dechiara, T.M.1    Estratiadis, A.2    Robertson, E.J.3
  • 30
    • 0026595355 scopus 로고
    • Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13
    • Dittrich B, Robinson WP, Knoblauch H, Buiting K, Schmidt K, et al. 1992. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13. Hum. Genet. 90:313-15
    • (1992) Hum. Genet. , vol.90 , pp. 313-315
    • Dittrich, B.1    Robinson, W.P.2    Knoblauch, H.3    Buiting, K.4    Schmidt, K.5
  • 31
    • 0024210659 scopus 로고
    • Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes
    • Donlon TA. 1988. Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes. Hum. Genet. 80:322-28
    • (1988) Hum. Genet. , vol.80 , pp. 322-328
    • Donlon, T.A.1
  • 32
    • 0022475535 scopus 로고
    • Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome
    • Donlon TA, Lalande M, Wyman A, Bruns G, Latt SA. 1986. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. Proc. Natl. Acad. USA 83:4408-12
    • (1986) Proc. Natl. Acad. USA , vol.83 , pp. 4408-4412
    • Donlon, T.A.1    Lalande, M.2    Wyman, A.3    Bruns, G.4    Latt, S.A.5
  • 33
    • 0026700732 scopus 로고
    • A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes
    • Driscoll DJ, Waters MF Williams, C.A., Zori RT, Glenn CC, Avidano KM, Nicholls RD. 1992. A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes. Genomics 13:917-24
    • (1992) Genomics , vol.13 , pp. 917-924
    • Driscoll, D.J.1    Waters, M.F.2    Williams, C.A.3    Zori, R.T.4    Glenn, C.C.5    Avidano, K.M.6    Nicholls, R.D.7
  • 34
    • 0028652716 scopus 로고
    • High-resolution replication bands compared with morphologic G- and R-bands
    • Drouin R, Holmquist GP, Richer CL. 1994. High-resolution replication bands compared with morphologic G- and R-bands. Adv. Hum. Genet. 22:47-115
    • (1994) Adv. Hum. Genet. , vol.22 , pp. 47-115
    • Drouin, R.1    Holmquist, G.P.2    Richer, C.L.3
  • 35
    • 0028218938 scopus 로고
    • Parental imprinting of autosomal mammalian genes
    • Efstratiadis A. 1994. Parental imprinting of autosomal mammalian genes. Curr. Opin. Genet. Dev. 4:265-80
    • (1994) Curr. Opin. Genet. Dev. , vol.4 , pp. 265-280
    • Efstratiadis, A.1
  • 36
    • 0028006662 scopus 로고
    • Parental imprinting and the IGF2 gene
    • Ekstrom TJ. 1994. Parental imprinting and the IGF2 gene. Horm. Res. 42:176-81
    • (1994) Horm. Res. , vol.42 , pp. 176-181
    • Ekstrom, T.J.1
  • 37
    • 0028899741 scopus 로고
    • Promoter-specific IGF2 imprinting status and its plasticity during human liver development
    • Ekstrom TJ, Cui H, Li X, Ohlsson R. 1995. Promoter-specific IGF2 imprinting status and its plasticity during human liver development. Development 121:309-16
    • (1995) Development , vol.121 , pp. 309-316
    • Ekstrom, T.J.1    Cui, H.2    Li, X.3    Ohlsson, R.4
  • 38
    • 0018939994 scopus 로고
    • A new genetic concept: Uniparental disomy and its potential effect, isodisomy
    • Engel E. 1980. A new genetic concept: uniparental disomy and its potential effect, isodisomy. Am. J. Med. Genet. 6:137-43
    • (1980) Am. J. Med. Genet. , vol.6 , pp. 137-143
    • Engel, E.1
  • 39
    • 0028841981 scopus 로고
    • Chromatin structure and imprinting: Developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene
    • Feil R, Handel MA, Allen ND, Reik W. 1995. Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene. Dev. Genet. 17:240-52
    • (1995) Dev. Genet. , vol.17 , pp. 240-252
    • Feil, R.1    Handel, Ma.2    Allen, N.D.3    Reik, W.4
  • 40
    • 0026428611 scopus 로고
    • Embryological and molecular investigations of parental imprinting on mouse chromosome 7
    • Ferguson-Smith AC, Cattanach BM, Barton SC, Beechey CV, Surani MA. 1991. Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 351:667-69
    • (1991) Nature , vol.351 , pp. 667-669
    • Ferguson-Smith, A.C.1    Cattanach, B.M.2    Barton, S.C.3    Beechey, C.V.4    Surani, M.A.5
  • 41
    • 0026516722 scopus 로고
    • Trans-sensing hypothesis for origin of Beckwith-Wiedemann syndrome
    • Fidler AE, Maw MA, Eccles MR, Reeve AE. 1992. Trans-sensing hypothesis for origin of Beckwith-Wiedemann syndrome. Lancet 339:243
    • (1992) Lancet , vol.339 , pp. 243
    • Fidler, A.E.1    Maw, M.A.2    Eccles, M.R.3    Reeve, A.E.4
  • 42
    • 0028319233 scopus 로고
    • No evidence for genomic imprinting of the human BCR gene
    • Fioretos T, Heisterkamp N, Groffen J. 1994. No evidence for genomic imprinting of the human BCR gene. Blood 83:3441-44
    • (1994) Blood , vol.83 , pp. 3441-3444
    • Fioretos, T.1    Heisterkamp, N.2    Groffen, J.3
  • 46
    • 0030052505 scopus 로고    scopus 로고
    • Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene
    • Glenn CC, Saitoh S, Jong MT, Filbrandt MM, Surti U, et al. 1996. Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. Am. J. Hum. Genet. 58:335-46
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 335-346
    • Glenn, C.C.1    Saitoh, S.2    Jong, M.T.3    Filbrandt, M.M.4    Surti, U.5
  • 47
    • 0028019677 scopus 로고
    • The critical region for Angelman syndrome lies between D15S122 and D15S113
    • Greger V, Reis A, Lalande M. 1994. The critical region for Angelman syndrome lies between D15S122 and D15S113. Am. J. Med. Genet. 53:396-98
    • (1994) Am. J. Med. Genet. , vol.53 , pp. 396-398
    • Greger, V.1    Reis, A.2    Lalande, M.3
  • 48
    • 0027217017 scopus 로고
    • Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient
    • Greger V, Woolf E, Lalande M. 1993. Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient. Hum. Mol. Genet. 2:921-24
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 921-924
    • Greger, V.1    Woolf, E.2    Lalande, M.3
  • 49
    • 0028933627 scopus 로고
    • Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region
    • Gunaratne PH, Nakao M, Ledbetter DH, Sutcliffe JS, Chinault AC. 1995. Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region. Genes Dev. 9:808-820
    • (1995) Genes Dev. , vol.9 , pp. 808-820
    • Gunaratne, P.H.1    Nakao, M.2    Ledbetter, D.H.3    Sutcliffe, J.S.4    Chinault, A.C.5
  • 50
    • 0026698262 scopus 로고
    • Parental origin of chromosomes involved in the translocation t(9;22)
    • Haas OA, Argyriou-Tirita A, Lion T. 1992. Parental origin of chromosomes involved in the translocation t(9;22). Nature 359:414-16
    • (1992) Nature , vol.359 , pp. 414-416
    • Haas, O.A.1    Argyriou-Tirita, A.2    Lion, T.3
  • 51
    • 0025360106 scopus 로고
    • Genomic imprinting: Review and relevance to human diseases
    • Hall JG. 1990. Genomic imprinting: review and relevance to human diseases. Am. J. Hum. Genet. 46:857-73
    • (1990) Am. J. Hum. Genet. , vol.46 , pp. 857-873
    • Hall, J.G.1
  • 54
    • 0028587166 scopus 로고
    • The genetics of Wilms' tumor - A case of disrupted development
    • Hastie ND. 1994. The genetics of Wilms' tumor - a case of disrupted development. Annu. Rev. Genet. 28:523-58
    • (1994) Annu. Rev. Genet. , vol.28 , pp. 523-558
    • Hastie, N.D.1
  • 55
    • 0029896367 scopus 로고    scopus 로고
    • Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors
    • 53a. Hatada I, Inazawa J, Abe T, Nakayama M, Kaneko Y, et al. 1996. Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors. Hum. Mol. Genet. 5:783-88
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 783-788
    • Hatada, I.1    Inazawa, J.2    Abe, T.3    Nakayama, M.4    Kaneko, Y.5
  • 56
    • 0028980026 scopus 로고
    • Genomic imprinting of p57KIP2, acyclin-dependent kinase inhibitor, in mouse
    • Hatada I, Mukai T. 1995. Genomic imprinting of p57KIP2, acyclin-dependent kinase inhibitor, in mouse. Nat. Genet. 11:204-6
    • (1995) Nat. Genet. , vol.11 , pp. 204-206
    • Hatada, I.1    Mukai, T.2
  • 58
  • 59
    • 0027793754 scopus 로고
    • Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: A post-fertilization event
    • Henry I, Puech A, Riesewijk A, Ahnine L, Mannens M, et al. 1993. Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event. Eur. J. Hum. Genet. 1:19-29
    • (1993) Eur. J. Hum. Genet. , vol.1 , pp. 19-29
    • Henry, I.1    Puech, A.2    Riesewijk, A.3    Ahnine, L.4    Mannens, M.5
  • 60
    • 0028142934 scopus 로고
    • Further localization of the gene for hereditary paragangliomas (PGL) and evidence for linkage in unrelated families
    • Heutink P, van der Mey AGL, Bardoel A, Breedveld G, Pertijs J, et al. 1994. Further localization of the gene for hereditary paragangliomas (PGL) and evidence for linkage in unrelated families. Eur. J. Hum. Genet. 2:148-58
    • (1994) Eur. J. Hum. Genet. , vol.2 , pp. 148-158
    • Heutink, P.1    Van Der Mey, A.G.L.2    Bardoel, A.3    Breedveld, G.4    Pertijs, J.5
  • 61
    • 0025886289 scopus 로고
    • Genomic imprinting in an Angelman and Prader-Willi translocation family
    • Hulten M, Armstrong S, Challinor P, Gould C, Hardy G, et al. 1991. Genomic imprinting in an Angelman and Prader-Willi translocation family. Lancet 338:638-39
    • (1991) Lancet , vol.338 , pp. 638-639
    • Hulten, M.1    Armstrong, S.2    Challinor, P.3    Gould, C.4    Hardy, G.5
  • 62
    • 0025891042 scopus 로고
    • Replication asynchrony between homologs 15q11.2: Cytogenetic evidence for genomic imprinting
    • Izumikawa Y, Naritomi K, Hirayama K. 1991. Replication asynchrony between homologs 15q11.2: cytogenetic evidence for genomic imprinting. Hum. Genet. 87:1-5
    • (1991) Hum. Genet. , vol.87 , pp. 1-5
    • Izumikawa, Y.1    Naritomi, K.2    Hirayama, K.3
  • 63
    • 0029043178 scopus 로고
    • Establishment of functional imprinting of the H19 gene in human developing placentae
    • Jinno Y, Ikeda Y, Yun K, Maw M, Masuzaki H, et al. 1995. Establishment of functional imprinting of the H19 gene in human developing placentae. Nat. Genet. 10:318-24
    • (1995) Nat. Genet. , vol.10 , pp. 318-324
    • Jinno, Y.1    Ikeda, Y.2    Yun, K.3    Maw, M.4    Masuzaki, H.5
  • 64
    • 0028342915 scopus 로고
    • Mosaic and polymorphic imprinting of the WT1 gene in humans
    • Jinno Y, Yun K, Nishiwaki K, Kubota T, Ogawa O, et al. 1994. Mosaic and polymorphic imprinting of the WT1 gene in humans. Nat. Genet. 6:305-9
    • (1994) Nat. Genet. , vol.6 , pp. 305-309
    • Jinno, Y.1    Yun, K.2    Nishiwaki, K.3    Kubota, T.4    Ogawa, O.5
  • 65
    • 0025995836 scopus 로고
    • Insulin-IGF2 region on chromosome 11 p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility
    • Julier C, Hyer RN, Davies J, Merlin F, Soularue P, et al. 1991. Insulin-IGF2 region on chromosome 11 p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility. Nature 354:155-59
    • (1991) Nature , vol.354 , pp. 155-159
    • Julier, C.1    Hyer, R.N.2    Davies, J.3    Merlin, F.4    Soularue, P.5
  • 66
    • 0026872675 scopus 로고
    • Beckwith-Wiedemann syndrome, tumourigenesis and imprinting
    • Junien C. 1992. Beckwith-Wiedemann syndrome, tumourigenesis and imprinting. Curr. Opin. Genet. Dev 2:431-38
    • (1992) Curr. Opin. Genet. Dev , vol.2 , pp. 431-438
    • Junien, C.1
  • 67
    • 0027180213 scopus 로고
    • The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans
    • Kalscheuer VM, Mariman EC, Schepens MT, Rehder H, Ropers HH. 1993. The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans. Nat. Genet. 5:74-78
    • (1993) Nat. Genet. , vol.5 , pp. 74-78
    • Kalscheuer, V.M.1    Mariman, E.C.2    Schepens, M.T.3    Rehder, H.4    Ropers, H.H.5
  • 68
    • 0023617404 scopus 로고
    • Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance
    • Kaplan LC, Wharton R, Elias E, Mandell F, Donlon T, Latt SA. 1987. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance. Am. J. Med. Genet. 28:55-53
    • (1987) Am. J. Med. Genet. , vol.28 , pp. 55-153
    • Kaplan, L.C.1    Wharton, R.2    Elias, E.3    Mandell, F.4    Donlon, T.5    Latt, S.A.6
  • 69
    • 0028879861 scopus 로고
    • Allele-specific replication timing in imprinted domains: Absence of asynchrony at several loci
    • Kawame H, Gartler SM, Hansen RS. 1995. Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci. Hum. Mol. Genet. 4:2287-93
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2287-2293
    • Kawame, H.1    Gartler, S.M.2    Hansen, R.S.3
  • 70
    • 0027205671 scopus 로고
    • Allele-specific replication timing of imprinted gene regions
    • Kitsberg D, Selig S, Brandeis M, Simon I, Keshet I, et al. 1994. Allele-specific replication timing of imprinted gene regions. Nature 364:459-63
    • (1994) Nature , vol.364 , pp. 459-463
    • Kitsberg, D.1    Selig, S.2    Brandeis, M.3    Simon, I.4    Keshet, I.5
  • 71
    • 0028260642 scopus 로고
    • Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region
    • Knoll JH, Cheng SD, Lalande M. 1994. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region. Nat. Genet. 6:41-46
    • (1994) Nat. Genet. , vol.6 , pp. 41-46
    • Knoll, J.H.1    Cheng, S.D.2    Lalande, M.3
  • 73
    • 0025292716 scopus 로고
    • Angelman syndrome: Three molecular classes identified with chromosome 15q11q13-specific DNA markers
    • Knoll JH, Nicholls RD, Magenis RE, Glatt K, Graham JM, et al. 1990. Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers. Am. J. Hum. Genet. 47:149-55
    • (1990) Am. J. Hum. Genet. , vol.47 , pp. 149-155
    • Knoll, J.H.1    Nicholls, R.D.2    Magenis, R.E.3    Glatt, K.4    Graham, J.M.5
  • 74
    • 0024619007 scopus 로고
    • Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
    • Knoll JH, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA. 1989. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am. J. Med. Genet. 32:285-90
    • (1989) Am. J. Med. Genet. , vol.32 , pp. 285-290
    • Knoll, J.H.1    Nicholls, R.D.2    Magenis, R.E.3    Graham, J.M.4    Lalande, M.5    Latt, S.A.6
  • 75
    • 0027231784 scopus 로고
    • Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from human chromosome 11
    • Koi M, Johnson AL, Kalikin LM, Little FP, Nakamura Y, et al. 1993. Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from human chromosome 11. Science 260:361-64
    • (1993) Science , vol.260 , pp. 361-364
    • Koi, M.1    Johnson, A.L.2    Kalikin, L.M.3    Little, F.P.4    Nakamura, Y.5
  • 76
    • 0029021151 scopus 로고
    • A molecular and cytogenetic study in Finnish Prader-Willi patients
    • Kokkonen H, Kahkonen M, Leisti J. 1995. A molecular and cytogenetic study in Finnish Prader-Willi patients. Hum. Genet. 95:568-71
    • (1995) Hum. Genet. , vol.95 , pp. 568-571
    • Kokkonen, H.1    Kahkonen, M.2    Leisti, J.3
  • 77
    • 0029869293 scopus 로고    scopus 로고
    • Selective maternal-allele loss in human lung cancer of the maternally expressed p57KIP2 gene at 11p15.5
    • 74a. Kondo M, Matsuoka S, Uchida K, Osada H, Nagatake M et al. 1996. Selective maternal-allele loss in human lung cancer of the maternally expressed p57KIP2 gene at 11p15.5. Oncogene 12:1365-68
    • (1996) Oncogene , vol.12 , pp. 1365-1368
    • Kondo, M.1    Matsuoka, S.2    Uchida, K.3    Osada, H.4    Nagatake, M.5
  • 78
    • 0028914364 scopus 로고
    • Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
    • Kotzot D, Schmitt S, Bernasconi F, Robinson WP, Lurie JW, et al. 1995. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Hum. Mol. Genet. 4:583-87
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 583-587
    • Kotzot, D.1    Schmitt, S.2    Bernasconi, F.3    Robinson, W.P.4    Lurie, J.W.5
  • 79
    • 0024517062 scopus 로고
    • Familial Wiedemann-Beckwith syndrome and a second Wilms' tumor locus both map to 11p15.5
    • Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, et al. 1989. Familial Wiedemann-Beckwith syndrome and a second Wilms' tumor locus both map to 11p15.5. Am. J. Hum. Genet. 44:711-19
    • (1989) Am. J. Hum. Genet. , vol.44 , pp. 711-719
    • Koufos, A.1    Grundy, P.2    Morgan, K.3    Aleck, K.A.4    Hadro, T.5
  • 80
    • 0021900245 scopus 로고
    • Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis
    • Lalande M, Schreck RR, Hoffman R, Latt S A. 1985. Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis. Cytometry 6:1-6
    • (1985) Cytometry , vol.6 , pp. 1-6
    • Lalande, M.1    Schreck, R.R.2    Hoffman, R.3    Latt, S.A.4
  • 81
    • 0028937174 scopus 로고
    • Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution
    • LaSalle JM, Lalande M. 1995. Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution. Nat. Genet. 9:386-94
    • (1995) Nat. Genet. , vol.9 , pp. 386-394
    • Lasalle, J.M.1    Lalande, M.2
  • 82
    • 0030043993 scopus 로고    scopus 로고
    • Homologous association of oppositely imprinted chromosomal domains
    • LaSalle JM, Lalande M. 1996. Homologous association of oppositely imprinted chromosomal domains. Science 272:725-28
    • (1996) Science , vol.272 , pp. 725-728
    • Lasalle, J.M.1    Lalande, M.2
  • 83
    • 0029162269 scopus 로고
    • Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
    • Ledbetter DH, Engel E. 1995. Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. Hum. Mol. Genet. 4:1757-64
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 1757-1764
    • Ledbetter, D.H.1    Engel, E.2
  • 85
    • 0027018063 scopus 로고
    • Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
    • Leff SE, Brannan CI, Reed ML, Ozcelik T, Francke U, et al. 1992. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat. Genet. 2:259-64
    • (1992) Nat. Genet. , vol.2 , pp. 259-264
    • Leff, S.E.1    Brannan, C.I.2    Reed, M.L.3    Ozcelik, T.4    Francke, U.5
  • 88
    • 0028868892 scopus 로고
    • Asynchronous DNA replication between 15q11.2q12 homologs: Cytogenetic evidence for maternal imprinting and delayed replication
    • Lin MS, Zhang A, Fujimoto A. 1995. Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication. Hum. Genet. 96:572-76
    • (1995) Hum. Genet. , vol.96 , pp. 572-576
    • Lin, M.S.1    Zhang, A.2    Fujimoto, A.3
  • 89
    • 0026539536 scopus 로고
    • Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours
    • Little MH, Dunn R, Byrne JA, Seawright A, Smith PJ, et al. 1992. Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours. Oncogene 7:635-41
    • (1992) Oncogene , vol.7 , pp. 635-641
    • Little, M.H.1    Dunn, R.2    Byrne, J.A.3    Seawright, A.4    Smith, P.J.5
  • 91
    • 0016389956 scopus 로고
    • Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome
    • Lubinsky M, Herrmann J, Kosseff AL, Opitz JM. 1974. Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome. Lancet 1:932
    • (1974) Lancet , vol.1 , pp. 932
    • Lubinsky, M.1    Herrmann, J.2    Kosseff, A.L.3    Opitz, J.M.4
  • 94
    • 0028316620 scopus 로고
    • Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
    • Mannens M, Hoovers JM, Redeker E, Verjaal M, Feinberg AP, et al. 1994. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. Eur. J. Hum. Genet. 2:3-23
    • (1994) Eur. J. Hum. Genet. , vol.2 , pp. 3-23
    • Mannens, M.1    Hoovers, J.M.2    Redeker, E.3    Verjaal, M.4    Feinberg, A.P.5
  • 95
    • 0024212964 scopus 로고
    • Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours
    • Mannens M, Slater RM, Heyting C, Bliek J, de Kraker J, et al. 1988. Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours. Hum. Genet. 81:41-48
    • (1988) Hum. Genet. , vol.81 , pp. 41-48
    • Mannens, M.1    Slater, R.M.2    Heyting, C.3    Bliek, J.4    De Kraker, J.5
  • 96
    • 0028970291 scopus 로고
    • Testing parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-x2 method
    • Margaritte-Jeannin P, Clerget-Darpoux F, Hors J, Deschamps I. 1995. Testing parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-x2 method. Am. J. Hum. Genet. 56:1080-87
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 1080-1087
    • Margaritte-Jeannin, P.1    Clerget-Darpoux, F.2    Hors, J.3    Deschamps, I.4
  • 97
    • 0028809123 scopus 로고
    • Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: Evidence for genetic heterogeneity
    • Mariman ECM, van Beersum SEC, Cremers CW R.J., Struycken PM, Ropers HH. 1995. Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity. Hum. Genet. 95:56-62
    • (1995) Hum. Genet. , vol.95 , pp. 56-62
    • Mariman, E.C.M.1    Van Beersum, S.E.C.2    Cremers, C.W.R.J.3    Struycken, P.M.4    Ropers, H.H.5
  • 98
    • 0026647855 scopus 로고
    • The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis
    • Mascari MJ, Gottlieb W, Rogan PK, Butler MG, Waller DA, et al. 1992. The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis. N. Engl. J. Med. 326:1599-607
    • (1992) N. Engl. J. Med. , vol.326 , pp. 1599-1607
    • Mascari, M.J.1    Gottlieb, W.2    Rogan, P.K.3    Butler, M.G.4    Waller, D.A.5
  • 99
    • 0029978017 scopus 로고    scopus 로고
    • Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15
    • 95a. Matsuoka S, Thompson JS, Edwards MC, Barletta JM, Grundy P, et al. 1996. Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15. Proc. Natl. Acad. Sci. USA 93:3026-30
    • (1996) Proc. Natl. Acad. Sci. USA , vol.93 , pp. 3026-3030
    • Matsuoka, S.1    Thompson, J.S.2    Edwards, M.C.3    Barletta, J.M.4    Grundy, P.5
  • 100
    • 0028988159 scopus 로고
    • p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
    • Matsuoka S, Edwards MC, Bai C, Parker S, Zhang P, et al. 1995, p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Dev. 9:650-62
    • (1995) Genes Dev. , vol.9 , pp. 650-662
    • Matsuoka, S.1    Edwards, M.C.2    Bai, C.3    Parker, S.4    Zhang, P.5
  • 101
    • 0020512319 scopus 로고
    • Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases
    • Mattei JF, Mattei MG, Giraud F. 1983. Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases. Hum. Genet. 64:356-62
    • (1983) Hum. Genet. , vol.64 , pp. 356-362
    • Mattei, J.F.1    Mattei, M.G.2    Giraud, F.3
  • 102
    • 0026077775 scopus 로고
    • Investigating genomic imprinting and susceptibility to insulin-dependent diabetes mellitus: An epidemiologic approach
    • McCarthy BJ, Dorman JS, Aston CE. 1991. Investigating genomic imprinting and susceptibility to insulin-dependent diabetes mellitus: an epidemiologic approach. Genet. Epidemiol. 8:177-86
    • (1991) Genet. Epidemiol. , vol.8 , pp. 177-186
    • McCarthy, B.J.1    Dorman, J.S.2    Aston, C.E.3
  • 103
    • 0021139084 scopus 로고
    • Completion of mouse embryogenesis requires both the maternal and paternal genomes
    • McGrath J, Solter D. 1984. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37:179-83
    • (1984) Cell , vol.37 , pp. 179-183
    • McGrath, J.1    Solter, D.2
  • 105
    • 0027048823 scopus 로고
    • Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome
    • Meijers-Heijboer EJ, Sandkuijl LA, Brunner HG, Smeets HJ, Hoogeboom AJ, et al. 1992. Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome. J. Med. Genet. 29:853-57
    • (1992) J. Med. Genet. , vol.29 , pp. 853-857
    • Meijers-Heijboer, E.J.1    Sandkuijl, L.A.2    Brunner, H.G.3    Smeets, H.J.4    Hoogeboom, A.J.5
  • 106
    • 0025958320 scopus 로고
    • Genomic imprinting in mammalian development: A parental tug-of-war
    • Moore T, Haig D. 1991. Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet. 7:45-49
    • (1991) Trends Genet. , vol.7 , pp. 45-49
    • Moore, T.1    Haig, D.2
  • 107
  • 108
    • 0026559276 scopus 로고
    • Beckwith-Wiedemann syndrome: A demonstration of the mechanisms responsible for the excess of transmitting females
    • Moutou C, Junien C, Henry I, Bonaiti-Pellie C. 1992. Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females. J. Med. Genet. 29:217-20
    • (1992) J. Med. Genet. , vol.29 , pp. 217-220
    • Moutou, C.1    Junien, C.2    Henry, I.3    Bonaiti-Pellie, C.4
  • 109
    • 0027787530 scopus 로고
    • A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene
    • Mutirangura A, Jayakumar A, Sutcliffe JS, Nakao M, McKinney MJ, et al. 1993. A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene. Genomics 18:546-52
    • (1993) Genomics , vol.18 , pp. 546-552
    • Mutirangura, A.1    Jayakumar, A.2    Sutcliffe, J.S.3    Nakao, M.4    McKinney, M.J.5
  • 110
    • 0027360049 scopus 로고
    • Oppositely imprinted genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast
    • 105a. Mutter GL, Stewart CL, Chaponot ML, Pomponio RJ. 1993. Oppositely imprinted genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast. Am. J. Hum. Genet. 53:1096-102
    • (1993) Am. J. Hum. Genet. , vol.53 , pp. 1096-1102
    • Mutter, G.L.1    Stewart, C.L.2    Chaponot, M.L.3    Pomponio, R.J.4
  • 111
    • 0028044579 scopus 로고
    • Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRN, E6-associated protein, and PAR-2 (D15S225E)
    • Nakao M, Sutcliffe JS, Durtschi B, Mutirangura A, Ledbetter DH, Beaudet AL. 1994. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRN, E6-associated protein, and PAR-2 (D15S225E). Hum. Mol. Genet. 3:309-15
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 309-315
    • Nakao, M.1    Sutcliffe, J.S.2    Durtschi, B.3    Mutirangura, A.4    Ledbetter, D.H.5    Beaudet, A.L.6
  • 113
    • 2442498402 scopus 로고
    • A cDNA from proximal human chromosome 15q maps near Mtv-1 on mouse chromosome 7
    • Nicholls RD. 1989. A cDNA from proximal human chromosome 15q maps near Mtv-1 on mouse chromosome 7. Mouse News Lett. 84:87-88
    • (1989) Mouse News Lett. , vol.84 , pp. 87-88
    • Nicholls, R.D.1
  • 114
    • 0024440608 scopus 로고
    • Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome
    • Nicholls RD, Knoll JH, Butler MG, Karam S, Lalande M. 1989. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature 342:281-85
    • (1989) Nature , vol.342 , pp. 281-285
    • Nicholls, R.D.1    Knoll, J.H.2    Butler, M.G.3    Karam, S.4    Lalande, M.5
  • 115
    • 0024397019 scopus 로고
    • Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome
    • Nicholls RD, Knoll JH, Glatt K, Hersh JH, Brewster TD, et al. 1989. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome. Am. J. Med. Genet. 33:76-77
    • (1989) Am. J. Med. Genet. , vol.33 , pp. 76-77
    • Nicholls, R.D.1    Knoll, J.H.2    Glatt, K.3    Hersh, J.H.4    Brewster, T.D.5
  • 116
    • 0021960375 scopus 로고
    • Clinical and cytogenetic studies of the Prader-Willi syndrome: Evidence of phenotype-karyotype correlation
    • Niikawa N, Ishikiriyama S. 1985. Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation. Hum. Genet. 69:22-27
    • (1985) Hum. Genet. , vol.69 , pp. 22-27
    • Niikawa, N.1    Ishikiriyama, S.2
  • 117
    • 0027285258 scopus 로고
    • Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
    • Ogawa O, Eccles MR, Szeto J, McNoe LA, Yun K, et al. 1993. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature 362:749-51
    • (1993) Nature , vol.362 , pp. 749-751
    • Ogawa, O.1    Eccles, M.R.2    Szeto, J.3    McNoe, L.A.4    Yun, K.5
  • 118
    • 0027749350 scopus 로고
    • Human insulin-like growth factor type I and type II receptors are not imprinted
    • 112a. Ogawa O, McNoe LA, Eccles MR, Morison IM, Reeve AE. 1993. Human insulin-like growth factor type I and type II receptors are not imprinted. Hum. Mol. Genet. 2:2163-65
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 2163-2165
    • Ogawa, O.1    McNoe, L.A.2    Eccles, M.R.3    Morison, I.M.4    Reeve, A.E.5
  • 119
    • 0028089079 scopus 로고
    • Overlapping patterns of IGF2 and H19 expression during human development: Biallelic IGF2 expression correlates with a lack of H19 expression
    • Ohlsson R, Hedborg F, Holmgren L, Walsh C, Ekstrom TJ. 1994. Overlapping patterns of IGF2 and H19 expression during human development: biallelic IGF2 expression correlates with a lack of H19 expression. Development 20:361-68
    • (1994) Development , vol.20 , pp. 361-368
    • Ohlsson, R.1    Hedborg, F.2    Holmgren, L.3    Walsh, C.4    Ekstrom, T.J.5
  • 120
    • 0027322519 scopus 로고
    • IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
    • Ohlsson R, Nystrom A, Pfeifer-Ohlsson S, Tohonen V, Hedborg F, et al. 1993. IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome. Nat. Genet. 4:94-97
    • (1993) Nat. Genet. , vol.4 , pp. 94-97
    • Ohlsson, R.1    Nystrom, A.2    Pfeifer-Ohlsson, S.3    Tohonen, V.4    Hedborg, F.5
  • 121
    • 0027026716 scopus 로고
    • Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region
    • Ozcelik T, Leff S, Robinson W, DonIon T, Lalande M, et al. 1992. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nat. Genet. 2:265-69
    • (1992) Nat. Genet. , vol.2 , pp. 265-269
    • Ozcelik, T.1    Leff, S.2    Robinson, W.3    Donion, T.4    Lalande, M.5
  • 123
    • 0027980337 scopus 로고
    • Allele-specific gene expression in mammals: The curious case of the imprinted RNAs
    • Pfeifer K, Tilghman SM. 1994. Allele-specific gene expression in mammals: the curious case of the imprinted RNAs. Genes Dev. 8:1867-74
    • (1994) Genes Dev. , vol.8 , pp. 1867-1874
    • Pfeifer, K.1    Tilghman, S.M.2
  • 125
    • 0000927260 scopus 로고
    • Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach Mytonieartigem zustand imneugeborenen Alter
    • Prader A, Labhart A, Willi H. 1956. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach Mytonieartigem zustand imneugeborenen Alter. Schweiz. Med. Wochenschr. 86:1260-61
    • (1956) Schweiz. Med. Wochenschr. , vol.86 , pp. 1260-1261
    • Prader, A.1    Labhart, A.2    Willi, H.3
  • 127
    • 0028286005 scopus 로고
    • DNA methylation and genomic imprinting
    • Razin A, Cedar H. 1994. DNA methylation and genomic imprinting. Cell 77:473-76
    • (1994) Cell , vol.77 , pp. 473-476
    • Razin, A.1    Cedar, H.2
  • 128
    • 0028959051 scopus 로고
    • Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3
    • Redeker E, Alders M, Hoovers JM, Richard CW, Westerveld A, Mannens M. 1985. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3. Cytogenet. Cell Genet. 68:222-25
    • (1985) Cytogenet. Cell Genet. , vol.68 , pp. 222-225
    • Redeker, E.1    Alders, M.2    Hoovers, J.M.3    Richard, C.W.4    Westerveld, A.5    Mannens, M.6
  • 129
    • 0028289468 scopus 로고
    • Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome
    • Reed ML, Leff SE. 1994. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome. Nat. Genet. 6:163-67
    • (1994) Nat. Genet. , vol.6 , pp. 163-167
    • Reed, M.L.1    Leff, S.E.2
  • 130
    • 0028862472 scopus 로고
    • Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain
    • Reik W, Brown KW, Schneid H, Le Bouc Y, Bickmore W, Maher ER. 1995. Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain. Hum. Mol. Genet. 4:2379-85
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2379-2385
    • Reik, W.1    Brown, K.W.2    Schneid, H.3    Le Bouc, Y.4    Bickmore, W.5    Maher, E.R.6
  • 132
    • 0028229959 scopus 로고
    • Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes
    • Reis A, Dittrich B, Greger V, Buiting K, Lalande M, et al. 1994. Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes. Am. J. Hum. Genet. 54:741-47
    • (1994) Am. J. Hum. Genet. , vol.54 , pp. 741-747
    • Reis, A.1    Dittrich, B.2    Greger, V.3    Buiting, K.4    Lalande, M.5
  • 133
    • 0027339103 scopus 로고
    • Exclusion of the GABAA-receptor beta 3 subunit gene as the Angelman's syndrome gene
    • Reis A, Kunze J, Ladanyi L, Enders H, Klein-Vogler U, Niemann G. 1993. Exclusion of the GABAA-receptor beta 3 subunit gene as the Angelman's syndrome gene. Lancet 341:122-23
    • (1993) Lancet , vol.341 , pp. 122-123
    • Reis, A.1    Kunze, J.2    Ladanyi, L.3    Enders, H.4    Klein-Vogler, U.5    Niemann, G.6
  • 134
    • 0030066202 scopus 로고    scopus 로고
    • Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription
    • 127a. Riesewijk AM, Schepens MT, Welch TR, van den Berg-Loonen EM, Mariman EM et al. 1996. Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription. Genomics 31:158-66
    • (1996) Genomics , vol.31 , pp. 158-166
    • Riesewijk, A.M.1    Schepens, M.T.2    Welch, T.R.3    Van Den Berg-Loonen, E.M.4    Mariman, E.M.5
  • 136
    • 0026353331 scopus 로고
    • Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients
    • Robinson WP, Bottani A, Xie YG, Balakrishman J, Binkert F, et al. 1991. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients. Am. J. Hum.Genet. 49:1219-34
    • (1991) Am. J. Hum.Genet. , vol.49 , pp. 1219-1234
    • Robinson, W.P.1    Bottani, A.2    Xie, Y.G.3    Balakrishman, J.4    Binkert, F.5
  • 137
    • 0028147055 scopus 로고
    • Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5
    • Sait SN, Nowak NJ, Singh-Kahlon P, Weksberg R, Squire J, et al. 1994. Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5. Genes Chromosom. Cancer 11:97-105
    • (1994) Genes Chromosom. Cancer , vol.11 , pp. 97-105
    • Sait, S.N.1    Nowak, N.J.2    Singh-Kahlon, P.3    Weksberg, R.4    Squire, J.5
  • 138
    • 0026500579 scopus 로고
    • Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene
    • Saitoh S, Kubota T, Ohta T, Jinno Y, Niikawa N, et al. 1992. Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene. Lancet 339:366-67
    • (1992) Lancet , vol.339 , pp. 366-367
    • Saitoh, S.1    Kubota, T.2    Ohta, T.3    Jinno, Y.4    Niikawa, N.5
  • 139
    • 0027231511 scopus 로고
    • Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome
    • Schneid H, Seurin D, Vazquez MP, Gourmelen M, Cabrol S, Le Bouc Y. 1993. Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome. J. Med. Genet. 30:353-62
    • (1993) J. Med. Genet. , vol.30 , pp. 353-362
    • Schneid, H.1    Seurin, D.2    Vazquez, M.P.3    Gourmelen, M.4    Cabrol, S.5    Le Bouc, Y.6
  • 142
    • 0025242074 scopus 로고
    • Genome imprinting phenomena on mouse chromosome 7
    • Searle AG, Beechey CV. 1990. Genome imprinting phenomena on mouse chromosome 7. Genet. Res. 56:37-244
    • (1990) Genet. Res. , vol.56 , pp. 37-244
    • Searle, A.G.1    Beechey, C.V.2
  • 143
    • 0027508152 scopus 로고
    • High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients
    • Sinnett D, Wagstaff J, Glatt K, Woolf E, Kirkness EJ, Lalande M. 1993. High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients. Am. J. Hum. Genet. 52:1216-29
    • (1993) Am. J. Hum. Genet. , vol.52 , pp. 1216-1229
    • Sinnett, D.1    Wagstaff, J.2    Glatt, K.3    Woolf, E.4    Kirkness, E.J.5    Lalande, M.6
  • 144
    • 0026566594 scopus 로고
    • Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15
    • Smeets DF, Hamel BC, Nelen MR, Smeets HJ, Bollen JH, et al. 1992. Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15. N. Engl. J. Med. 326:807-11
    • (1992) N. Engl. J. Med. , vol.326 , pp. 807-811
    • Smeets, D.F.1    Hamel, B.C.2    Nelen, M.R.3    Smeets, H.J.4    Bollen, J.H.5
  • 145
    • 0028864462 scopus 로고
    • Conservation of a maternal-specific methylation signal at the human IGF2R locus
    • 137a. Smrzka OW, Fae I, Stoger R, Kurzbauer R, Fischer GF, et al. 1995. Conservation of a maternal-specific methylation signal at the human IGF2R locus. Hum. Mol. Genet. 4:1945-52
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 1945-1952
    • Smrzka, O.W.1    Fae, I.2    Stoger, R.3    Kurzbauer, R.4    Fischer, G.F.5
  • 146
    • 0024152982 scopus 로고
    • Differential imprinting and expression of maternal and paternal genomes
    • Solter D. 1988. Differential imprinting and expression of maternal and paternal genomes. Annu. Rev. Genet. 22:127-46
    • (1988) Annu. Rev. Genet. , vol.22 , pp. 127-146
    • Solter, D.1
  • 148
    • 0028356544 scopus 로고
    • Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
    • Steenman MJ, Rainier S, Dobry CJ, Grundy P, Horon IL, Feinberg AP. 1994. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour. Nat. Genet. 7:433-39
    • (1994) Nat. Genet. , vol.7 , pp. 433-439
    • Steenman, M.J.1    Rainier, S.2    Dobry, C.J.3    Grundy, P.4    Horon, I.L.5    Feinberg, A.P.6
  • 149
    • 0029985822 scopus 로고    scopus 로고
    • Breakage in the SNRPN locus in a balanced translocation 46,XY,t(15;19) Prader-Willi syndrome patient
    • 140a. Sun Y, Nicholls RD, Butler MG, Saitoh S, Hainline BE, Palmer CG. 1996. Breakage in the SNRPN locus in a balanced translocation 46,XY,t(15;19) Prader-Willi syndrome patient. Hum. Mol. Genet. 5:517-24
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 517-524
    • Sun, Y.1    Nicholls, R.D.2    Butler, M.G.3    Saitoh, S.4    Hainline, B.E.5    Palmer, C.G.6
  • 150
    • 0021237658 scopus 로고
    • Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
    • Surani MAH, Carton SC, Norris ML. 1984. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature 308:548-50
    • (1984) Nature , vol.308 , pp. 548-550
    • Surani, M.A.H.1    Carton, S.C.2    Norris, M.L.3
  • 151
    • 0028133293 scopus 로고
    • Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
    • Sutcliffe JS, Nakao M, Christian S, Orstavik KH, Tommerup N, et al. 1994. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nat. Genet. 8:52-58
    • (1994) Nat. Genet. , vol.8 , pp. 52-58
    • Sutcliffe, J.S.1    Nakao, M.2    Christian, S.3    Orstavik, K.H.4    Tommerup, N.5
  • 152
    • 0029621799 scopus 로고
    • Allele-specific expression and total expression levels of imprinted genes during early mouse development: Implications for imprinting mechanisms
    • Szabo PE, Mann JR. 1995. Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms. Genes Devel. 9:3097-108
    • (1995) Genes Devel. , vol.9 , pp. 3097-3108
    • Szabo, P.E.1    Mann, J.R.2
  • 154
    • 0028935017 scopus 로고
    • Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms' tumor
    • Taniguchi T, Sullivan MJ, Ogawa O, Reeve AE. 1995. Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms' tumor. Proc. Natl. Acad. Sci. USA 92:2159-63
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 2159-2163
    • Taniguchi, T.1    Sullivan, M.J.2    Ogawa, O.3    Reeve, A.E.4
  • 155
    • 0026335165 scopus 로고
    • Escape from genomic imprinting at the mouse T-associated maternal effect (Tme) locus
    • Tsai J-Y, Silver LM. 1991. Escape from genomic imprinting at the mouse T-associated maternal effect (Tme) locus. Genetics 129:1159-66
    • (1991) Genetics , vol.129 , pp. 1159-1166
    • Tsai, J.-Y.1    Silver, L.M.2
  • 158
    • 0028224130 scopus 로고
    • Genomic imprinting - Defusing the ovarian time bomb
    • Varmuza S, Mann M. 1994. Genomic imprinting - defusing the ovarian time bomb. Trends Genet. 10:118-23
    • (1994) Trends Genet. , vol.10 , pp. 118-123
    • Varmuza, S.1    Mann, M.2
  • 159
    • 0026587756 scopus 로고
    • Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome
    • Viljoen D, Ramesar R. 1992. Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome. J. Med. Genet. 29:221-25
    • (1992) J. Med. Genet. , vol.29 , pp. 221-225
    • Viljoen, D.1    Ramesar, R.2
  • 160
    • 0027945263 scopus 로고
    • Promoter-specific imprinting of the human insulin-like growth factor-II gene
    • Vu TH, Hoffman AR. 1994. Promoter-specific imprinting of the human insulin-like growth factor-II gene. Nature 371:714-17
    • (1994) Nature , vol.371 , pp. 714-717
    • Vu, T.H.1    Hoffman, A.R.2
  • 161
    • 0026893703 scopus 로고
    • Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression
    • Wagstaff J, Knoll JH, Glatt KA, Shugart YY, Sommer A, Lalande M. 1992. Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression. Nat. Genet. 1:291-94
    • (1992) Nat. Genet. , vol.1 , pp. 291-294
    • Wagstaff, J.1    Knoll, J.H.2    Glatt, K.A.3    Shugart, Y.Y.4    Sommer, A.5    Lalande, M.6
  • 163
    • 0028935151 scopus 로고
    • Paternally derived H19 is differentially expressed in malignant and nonmalignant trophoblast
    • Walsh C, Miller SJ, Flam F, Fisher RA, Ohlsson R. 1995. Paternally derived H19 is differentially expressed in malignant and nonmalignant trophoblast. Cancer Res. 55:1111-16
    • (1995) Cancer Res. , vol.55 , pp. 1111-1116
    • Walsh, C.1    Miller, S.J.2    Flam, F.3    Fisher, R.A.4    Ohlsson, R.5
  • 164
    • 0027420362 scopus 로고
    • Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
    • Weksberg R, Shen DR, Fei YL, Song QL, Squire J. 1993. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nat. Genet. 5:143-50
    • (1993) Nat. Genet. , vol.5 , pp. 143-150
    • Weksberg, R.1    Shen, D.R.2    Fei, Y.L.3    Song, Q.L.4    Squire, J.5
  • 165
    • 0027289089 scopus 로고
    • Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted
    • Weksberg R, Teshima I, Williams BR, Greenberg CR, Pueschel SM, et al. 1993. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. Hum. Mol. Genet. 2:549-56
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 549-556
    • Weksberg, R.1    Teshima, I.2    Williams, B.R.3    Greenberg, C.R.4    Pueschel, S.M.5
  • 166
    • 0028124726 scopus 로고
    • Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
    • Wevrick R, Kerns JA, Francke U. 1994. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum. Mol. Genet. 3:1877-82
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1877-1882
    • Wevrick, R.1    Kerns, J.A.2    Francke, U.3
  • 167
    • 76549164702 scopus 로고
    • Complexe malformatif familial avec hernie ombilicale et macroglossie - Un "Syndrome Nouveau"?
    • Wiedemann HR. 1964. Complexe malformatif familial avec hernie ombilicale et macroglossie - un "Syndrome Nouveau"? J. Genet. Hum. 13:33-232
    • (1964) J. Genet. Hum. , vol.13 , pp. 33-232
    • Wiedemann, H.R.1
  • 168
    • 0023831210 scopus 로고
    • Genomic imprinting and carcinogenesis
    • Wilkins RJ. 1988. Genomic imprinting and carcinogenesis. Lancet 1:329-31
    • (1988) Lancet , vol.1 , pp. 329-331
    • Wilkins, R.J.1
  • 169
    • 0025052050 scopus 로고
    • Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting
    • Williams CA, Zori RT, Stone JW, Gray BA, Cantu ES, Ostrer H. 1990. Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting. Am. J. Med. Genet. 35:350-53
    • (1990) Am. J. Med. Genet. , vol.35 , pp. 350-353
    • Williams, C.A.1    Zori, R.T.2    Stone, J.W.3    Gray, B.A.4    Cantu, E.S.5    Ostrer, H.6
  • 170
  • 171
    • 0026922595 scopus 로고
    • Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2
    • Zemel S, Bartolomei MS, Tilghman SM. 1992. Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2. Nat. Genet. 2:61-65
    • (1992) Nat. Genet. , vol.2 , pp. 61-65
    • Zemel, S.1    Bartolomei, M.S.2    Tilghman, S.M.3
  • 172
    • 0028880765 scopus 로고
    • Concordant loss of imprinting of the human insulin-like growth factor II gene promoters in cancer
    • Zhan S, Shapiro D, Zhan S, Zhang L, Hirshfeld S, et al. 1995. Concordant loss of imprinting of the human insulin-like growth factor II gene promoters in cancer. J. Biol. Chem. 270:27983-86
    • (1995) J. Biol. Chem. , vol.270 , pp. 27983-27986
    • Zhan, S.1    Shapiro, D.2    Zhan, S.3    Zhang, L.4    Hirshfeld, S.5
  • 173
    • 0027496294 scopus 로고
    • Imprinting of human H19: Allele-specific CpG methylation, loss of the active allele in Wilms' tumor, and potential for somatic allele switching
    • Zhang Y, Shields T, Crenshaw T, Hao Y, Moulton T, Tycko B. 1993. Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms' tumor, and potential for somatic allele switching. Am. J. Hum. Genet. 53:113-24
    • (1993) Am. J. Hum. Genet. , vol.53 , pp. 113-124
    • Zhang, Y.1    Shields, T.2    Crenshaw, T.3    Hao, Y.4    Moulton, T.5    Tycko, B.6
  • 174
    • 0026849544 scopus 로고
    • Monoallelic expression of the human H19 gene
    • Zhang Y, Tycko B. 1992. Monoallelic expression of the human H19 gene. Nat. Genet. 1:40-44
    • (1992) Nat. Genet. , vol.1 , pp. 40-44
    • Zhang, Y.1    Tycko, B.2


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