-
1
-
-
0027280881
-
Methylation and imprinting: From host defense to gene regulation?
-
Barlow DP, 1993. Methylation and imprinting: from host defense to gene regulation? Science 260: 309-310.
-
(1993)
Science
, vol.260
, pp. 309-310
-
-
Barlow, D.P.1
-
2
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the igf2 gene
-
Bell AC, Felsenfeld G, 2000. Methylation of a CTCF-dependent boundary controls imprinted expression of the igf2 gene. Nature 405: 482-485.
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
3
-
-
0032890848
-
Assessment of SNRPN expression as a molecular tool in the diagnosis of Prader-Willi syndrome
-
Carrel AL, Huber S, Allen DxB, Voelkerding KV, 1999. Assessment of SNRPN expression as a molecular tool in the diagnosis of Prader-Willi syndrome. Mol Diagnos 4: 5-10.
-
(1999)
Mol Diagnos
, vol.4
, pp. 5-10
-
-
Carrel, A.L.1
Huber, S.2
Allen, Dx.B.3
Voelkerding, K.V.4
-
4
-
-
0000095385
-
X-inactivation in marsupials and monotremes
-
Cooper DP, Johnston G, Watson J M, Graves JAM, 1993. X-inactivation in marsupials and monotremes. Semin Develop Biol 4: 117-128
-
(1993)
Semin Develop Biol
, vol.4
, pp. 117-128
-
-
Cooper, D.P.1
Johnston, G.2
Watson, J.M.3
Graves, J.A.M.4
-
5
-
-
0031844174
-
Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: Association with aberrant phenotypes
-
Dean W, Bowden L, Aitchison A, Klose J, Moore T, Meneses JJ, Reik W, Feil R, 1998. Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes. Development 125(12): 2273-2282.
-
(1998)
Development
, vol.125
, Issue.12
, pp. 2273-2282
-
-
Dean, W.1
Bowden, L.2
Aitchison, A.3
Klose, J.4
Moore, T.5
Meneses, J.J.6
Reik, W.7
Feil, R.8
-
6
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
De Chiara T M, Robertson E J, Esfratadis A, 1991. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64: 849-859.
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
De Chiara, T.M.1
Robertson, E.J.2
Esfratadis, A.3
-
7
-
-
0034608797
-
Genome-wide scan for body composition in pigs reveals important role of imprinting
-
De Konning DJ, Rattink AP, Harlizus B, Van Arendonk JAM, Brascamp EW, Groenen MAM, 2000. Genome-wide scan for body composition in pigs reveals important role of imprinting. Proc Nat Acad Sci USA, 97: 7947-7950.
-
(2000)
Proc Nat Acad Sci USA
, vol.97
, pp. 7947-7950
-
-
De Konning, D.J.1
Rattink, A.P.2
Harlizus, B.3
Van Arendonk, J.A.M.4
Brascamp, E.W.5
Groenen, M.A.M.6
-
8
-
-
0034112603
-
Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo
-
Doherty AS, Mann MR, Tremblay KD, Bartolomei MS, Schultz RM, 2000. Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo. Biol Reprod 62(6): 1526-1535.
-
(2000)
Biol Reprod
, vol.62
, Issue.6
, pp. 1526-1535
-
-
Doherty, A.S.1
Mann, M.R.2
Tremblay, K.D.3
Bartolomei, M.S.4
Schultz, R.M.5
-
9
-
-
0027937839
-
Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes
-
Feil R, Walter J, Allen ND, Reik W, 1994. Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes. Development 120(10): 2933-2943.
-
(1994)
Development
, vol.120
, Issue.10
, pp. 2933-2943
-
-
Feil, R.1
Walter, J.2
Allen, N.D.3
Reik, W.4
-
10
-
-
0036799595
-
Identification of the single base change causing the callipyge muscle hypertrophy phenotype, the only known example of polar overdominance in mammals
-
Freking B, Murphy S, Wylie A, Rhodes SJ, Keele JW, Leymaster KA, et al. 2002. Identification of the single base change causing the callipyge muscle hypertrophy phenotype, the only known example of polar overdominance in mammals. Genome Research 12(10): 1496-1506.
-
(2002)
Genome Research
, vol.12
, Issue.10
, pp. 1496-1506
-
-
Freking, B.1
Murphy, S.2
Wylie, A.3
Rhodes, S.J.4
Keele, J.W.5
Leymaster, K.A.6
-
11
-
-
0028815477
-
Genomic imprinting of Mash2, a mouse gene required for trophoblast development
-
Guillemot F, Caspary T, Tilghman SM, Copeland NG, Gilbert DJ, Jenkins NA, et al. 1995. Genomic imprinting of Mash2, a mouse gene required for trophoblast development. Nat Genet 9: 235-242.
-
(1995)
Nat Genet
, vol.9
, pp. 235-242
-
-
Guillemot, F.1
Caspary, T.2
Tilghman, S.M.3
Copeland, N.G.4
Gilbert, D.J.5
Jenkins, N.A.6
-
12
-
-
10444266466
-
A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russel syndrome delimits a candidate gene region
-
Hannula K, Lipsanen-Nyman M, Kontiokari T, Kere J, 2001. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russel syndrome delimits a candidate gene region. Hum Mol Genet 9: 1587-1595.
-
(2001)
Hum Mol Genet
, vol.9
, pp. 1587-1595
-
-
Hannula, K.1
Lipsanen-Nyman, M.2
Kontiokari, T.3
Kere, J.4
-
13
-
-
0025738681
-
Uniparental disomy in a genetic cancer-predisposing syndrome
-
Henry I, Bonaiti-Pellie C, Chehensse V, Beldjord C, Schwartz C, Utermann G, Junien C, 1991. Uniparental disomy in a genetic cancer-predisposing syndrome. Nature 351: 665-667.
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henry, I.1
Bonaiti-Pellie, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
Utermann, G.6
Junien, C.7
-
14
-
-
0036792031
-
Abnormal gene expression in cloned mice derived from embryonic stem cell and cumulus cell nuclei
-
Humpherys D, Eggan K, Akutsu H, Friedman A, Hochedlinger K, Yanagimachi R, et al. 2002. Abnormal gene expression in cloned mice derived from embryonic stem cell and cumulus cell nuclei. Proc Natl Acad Sci USA 99(20): 12889-12894.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, Issue.20
, pp. 12889-12894
-
-
Humpherys, D.1
Eggan, K.2
Akutsu, H.3
Friedman, A.4
Hochedlinger, K.5
Yanagimachi, R.6
-
15
-
-
0032931894
-
An imprinted QTL with major effect on muscle mass and fat deposition maps to the IGF2 locus in pigs
-
Jeon JT, Carlborg Ö, Törnsten A, Giuffra E, Amerger V, Chardon P, et al. 1999. An imprinted QTL with major effect on muscle mass and fat deposition maps to the IGF2 locus in pigs. Nat Genetics 21: 155-156.
-
(1999)
Nat Genetics
, vol.21
, pp. 155-156
-
-
Jeon, J.T.1
Carlborg, Ö.2
Törnsten, A.3
Giuffra, E.4
Amerger, V.5
Chardon, P.6
-
16
-
-
0027180213
-
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 H, 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.5
-
17
-
-
0032963598
-
Parental allele specific chromatin configuration in a boundary imprinting-control element upstream of the mouse H19 gene
-
Khosla S, Aitchison A, Gregory R, Allen ND, Freil R, 1999. Parental allele specific chromatin configuration in a boundary imprinting-control element upstream of the mouse H19 gene. Mol Cell Biol 19: 2556-2566.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 2556-2566
-
-
Khosla, S.1
Aitchison, A.2
Gregory, R.3
Allen, N.D.4
Freil, R.5
-
18
-
-
0035880496
-
Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary
-
Killian JK, Nolan CM, Wylie AA, Li T, Vu TH, Hoffman AR, Jirtle RL, 2001a. Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary. Hum Mol Genet 10(17): 1721-1728.
-
(2001)
Hum Mol Genet
, vol.10
, Issue.17
, pp. 1721-1728
-
-
Killian, J.K.1
Nolan, C.M.2
Wylie, A.A.3
Li, T.4
Vu, T.H.5
Hoffman, A.R.6
Jirtle, R.L.7
-
19
-
-
0035881681
-
Monotreme IGF2 expression and ancestral origin of genomic imprinting
-
Killian JK, Nolan CM, Stewart N, Munday BL, Andersen NA, Nicol S, Jirtle RL, 2001b. Monotreme IGF2 expression and ancestral origin of genomic imprinting. J Exp Zool 291: 205-212.
-
(2001)
J Exp Zool
, vol.291
, pp. 205-212
-
-
Killian, J.K.1
Nolan, C.M.2
Stewart, N.3
Munday, B.L.4
Andersen, N.A.5
Nicol, S.6
Jirtle, R.L.7
-
20
-
-
0024619007
-
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 Jr., Lalande M, Latt SA, 1989. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Amer J Med Genet 32: 285-290.
-
(1989)
Amer J Med Genet
, vol.32
, pp. 285-290
-
-
Knoll, J.H.1
Nicholls, R.D.2
Magenis, R.E.3
Graham Jr., J.M.4
Lalande, M.5
Latt, S.A.6
-
21
-
-
1942531259
-
Birth of parthenogenetic mice that can develop to adulthood
-
Kono T, Obata Y, Wu Q, Niwa K, Ono Y, Yamamoto Y, et al. 2004. Birth of parthenogenetic mice that can develop to adulthood. Nature 428: 860-864.
-
(2004)
Nature
, vol.428
, pp. 860-864
-
-
Kono, T.1
Obata, Y.2
Wu, Q.3
Niwa, K.4
Ono, Y.5
Yamamoto, Y.6
-
22
-
-
0024517062
-
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p11.5
-
Koufos A, Grundy P, Morgan K, Alech KA, Hadro T, Lampkin BC, 1989. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p11.5. Amer J Med Genet 44: 711-719.
-
(1989)
Amer J Med Genet
, vol.44
, pp. 711-719
-
-
Koufos, A.1
Grundy, P.2
Morgan, K.3
Alech, K.A.4
Hadro, T.5
Lampkin, B.C.6
-
23
-
-
0031820331
-
X-Chromosome inactivation: A repeat hypothesis Cytogenet
-
Lyon MF 1998. X-Chromosome inactivation: a repeat hypothesis Cytogenet. Cell Genet 80: 133-137.
-
(1998)
Cell Genet
, vol.80
, pp. 133-137
-
-
Lyon, M.F.1
-
24
-
-
0027018063
-
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, Copeland NG, Jenkins NA, 1992. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat Genet 2(4): 259-264.
-
(1992)
Nat Genet
, vol.2
, Issue.4
, pp. 259-264
-
-
Leff, S.E.1
Brannan, C.I.2
Reed, M.L.3
Ozcelik, T.4
Francke, U.5
Copeland, N.G.6
Jenkins, N.A.7
-
25
-
-
0034816108
-
Evidence against GRB10 as the gene responsible for Silver-Russell syndrome
-
Mc Cann JA, Zheng H, Islam A, Goodyer CG, Polychronakos C, 2001. Evidence against GRB10 as the gene responsible for Silver-Russell syndrome. Biochem Biophys Res Commun 286: 943-948.
-
(2001)
Biochem Biophys Res Commun
, vol.286
, pp. 943-948
-
-
Mc Cann, J.A.1
Zheng, H.2
Islam, A.3
Goodyer, C.G.4
Polychronakos, C.5
-
26
-
-
0033940412
-
Duplication of 7p11.2-p13, including GRB10, in Silver-Russel syndrome
-
Monk D, Wakeling EL, Proud V, Hitchins M, Abu-Amero SN, Stanier P, 2000. Duplication of 7p11.2-p13, including GRB10, in Silver-Russel syndrome. Amer J Hum Genet 66: 36-46.
-
(2000)
Amer J Hum Genet
, vol.66
, pp. 36-46
-
-
Monk, D.1
Wakeling, E.L.2
Proud, V.3
Hitchins, M.4
Abu-Amero, S.N.5
Stanier, P.6
-
27
-
-
0025958320
-
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
-
28
-
-
0032909094
-
A paternally expressed QTL affecting skeletal and cardiac muscle mass in pigs maps to the IGF2 locus
-
Nezer C, Moreau L, Brouwers B, Coppieters W, Detilleux J, Hanset R, et al. 1999. A paternally expressed QTL affecting skeletal and cardiac muscle mass in pigs maps to the IGF2 locus. Nat Genet 21: 157-158.
-
(1999)
Nat Genet
, vol.21
, pp. 157-158
-
-
Nezer, C.1
Moreau, L.2
Brouwers, B.3
Coppieters, W.4
Detilleux, J.5
Hanset, R.6
-
29
-
-
0034851701
-
Imprint status of M6P/IGF2R and IGF2 in chickens
-
Nolan CM, Killian JK, Petitte JN, Jirtle RL, 2001. Imprint status of M6P/IGF2R and IGF2 in chickens. Dev Genes Evol 211: 179-183.
-
(2001)
Dev Genes Evol
, vol.211
, pp. 179-183
-
-
Nolan, C.M.1
Killian, J.2
Petitte, J.N.3
Jirtle, R.L.4
-
30
-
-
0027749350
-
Human insulin-like growth factor type I and type II receptors are not imprinted
-
Ogawa O, Mc Noe 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: 2163-2165.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2163-2165
-
-
Ogawa, O.1
Mc Noe, L.A.2
Eccles, M.R.3
Morison, I.M.4
Reeve, A.E.5
-
31
-
-
0035336255
-
Allelic Igf2r repression does not correlate with expression of antisense RNA in human extra-embryonic tissues
-
Oudejans CB, Westerman B, Wouters D, Goodyear S, Leegwater PA, Van Wijk IL, Sleutels F, 2001. Allelic Igf2r repression does not correlate with expression of antisense RNA in human extra-embryonic tissues. Genomics 73: 331-337.
-
(2001)
Genomics
, vol.73
, pp. 331-337
-
-
Oudejans, C.B.1
Westerman, B.2
Wouters, D.3
Goodyear, S.4
Leegwater, P.A.5
Van Wijk, I.L.6
Sleutels, F.7
-
32
-
-
0037338544
-
The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domains
-
Pant V, Mariano P, Kanduri C, Mattson A, Lobanenkov VV, Heuchel R, Ohlsson R, 2003. The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domains. Gene Dev 17(5): 586-590.
-
(2003)
Gene Dev
, vol.17
, Issue.5
, pp. 586-590
-
-
Pant, V.1
Mariano, P.2
Kanduri, C.3
Mattson, A.4
Lobanenkov, V.V.5
Heuchel, R.6
Ohlsson, R.7
-
33
-
-
0031228039
-
The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain
-
Rougeulle C, Glatt H, Lalande M, 1997. The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Nat Genet 17: 14-15.
-
(1997)
Nat Genet
, vol.17
, pp. 14-15
-
-
Rougeulle, C.1
Glatt, H.2
Lalande, M.3
-
34
-
-
0032129473
-
Angelman syndrome: How many genes to remain silent?
-
Rougeulle C, Lalande M, 1998. Angelman syndrome: how many genes to remain silent? Neurogenetics 1: 229-237.
-
(1998)
Neurogenetics
, vol.1
, pp. 229-237
-
-
Rougeulle, C.1
Lalande, M.2
-
35
-
-
0030886796
-
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
-
Shemer R, Birger Y, Riggs AD, Razin A, 1997. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc Nat Acad Sci USA, 94: 10267-10272.
-
(1997)
Proc Nat Acad Sci USA
, vol.94
, pp. 10267-10272
-
-
Shemer, R.1
Birger, Y.2
Riggs, A.D.3
Razin, A.4
-
36
-
-
0027400888
-
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
-
Stoger R, Kubicka P, Liu C-G, Kafri T, Razin A, Cedar H, Barlow DP, 1993. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. Cell 73: 61-71.
-
(1993)
Cell
, vol.73
, pp. 61-71
-
-
Stoger, R.1
Kubicka, P.2
Liu, C.-G.3
Kafri, T.4
Razin, A.5
Cedar, H.6
Barlow, D.P.7
-
37
-
-
4243192491
-
Characterization of quantitative trait loci for growth and meat quality in a cross between commercial breeds of swine
-
Thomsen H, Lee HK, Rothschild MF, Malek M, Dekkers JC, 2004. Characterization of quantitative trait loci for growth and meat quality in a cross between commercial breeds of swine. J Anim Sci 82(8): 2213-2228.
-
(2004)
J Anim Sci
, vol.82
, Issue.8
, pp. 2213-2228
-
-
Thomsen, H.1
Lee, H.K.2
Rothschild, M.F.3
Malek, M.4
Dekkers, J.C.5
-
38
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen JL, Duran KL, Bartolomei MS, 1998. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Dev 12(23): 3693-3702.
-
(1998)
Genes Dev
, vol.12
, Issue.23
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
39
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
-
Tremblay KD, Saam JR, Ingram RS, Tilghman SM, Bartolomei MS, 1995. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nat Genet 9: 407-413.
-
(1995)
Nat Genet
, vol.9
, pp. 407-413
-
-
Tremblay, K.D.1
Saam, J.R.2
Ingram, R.S.3
Tilghman, S.M.4
Bartolomei, M.S.5
-
40
-
-
0030802395
-
A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
-
Tremblay KD, Duran KL, Bartolomei MS, 1997. A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol Cell Biol 17: 4322-4329.
-
(1997)
Mol Cell Biol
, vol.17
, pp. 4322-4329
-
-
Tremblay, K.D.1
Duran, K.L.2
Bartolomei, M.S.3
-
41
-
-
0242363235
-
A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig
-
Van Laere S, Nguyen M, Braunschweig M, Nezer C, Collette C, Moreau L, et al. 2003. A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig. Nature 23; 425(6960): 832-836.
-
(2003)
Nature 23
, vol.425
, Issue.6960
, pp. 832-836
-
-
Van Laere, S.1
Nguyen, M.2
Braunschweig, M.3
Nezer, C.4
Collette, C.5
Moreau, L.6
-
42
-
-
0028224130
-
Genomic imprinting defusing the ovarian time bomb
-
Varmuza S, Mann M, 1994. Genomic imprinting defusing the ovarian time bomb. Trends Genet 10(4): 118.
-
(1994)
Trends Genet
, vol.10
, Issue.4
, pp. 118
-
-
Varmuza, S.1
Mann, M.2
-
43
-
-
0031741651
-
Genomic imprinting is disrupted in interspecific Peromyscus hybrids
-
Vrana PB, Guan XJ, Ingram RS, Tilghman SM, 1998. Genomic imprinting is disrupted in interspecific Peromyscus hybrids. Nat Genet 20(4): 362-365.
-
(1998)
Nat Genet
, vol.20
, Issue.4
, pp. 362-365
-
-
Vrana, P.B.1
Guan, X.J.2
Ingram, R.S.3
Tilghman, S.M.4
-
44
-
-
0141960164
-
The potential role of gene duplications in the evolution of imprinting mechanisms
-
Walter J, Paulsen M, 2003. The potential role of gene duplications in the evolution of imprinting mechanisms. Hum Mol Genet 12: 215-220.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 215-220
-
-
Walter, J.1
Paulsen, M.2
-
45
-
-
0035111294
-
Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: Relation to expression and imprinting
-
Weber M, Milligan L, Delalbre A, Antoine E, Brunel C, Cathala G, Forn T, 2001. Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting. Mech Dev 101(1-2): 133-141.
-
(2001)
Mech Dev
, vol.101
, Issue.1-2
, pp. 133-141
-
-
Weber, M.1
Milligan, L.2
Delalbre, A.3
Antoine, E.4
Brunel, C.5
Cathala, G.6
Forn, T.7
-
46
-
-
0027420362
-
Disruption of insulin-like growth factor imprinting in Beckwith-Wiedemann syndrome
-
Weksberg R, Shen DR, Fei Song Q L, Squire J, 1993. Disruption of insulin-like growth factor imprinting in Beckwith-Wiedemann syndrome. Nat Genet 5: 143-150.
-
(1993)
Nat Genet
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei Song, Q.L.3
Squire, J.4
|