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Volumn 60, Issue 3, 1997, Pages 597-604

Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 7P; CHROMOSOME MAP; CLINICAL ARTICLE; DNA POLYMORPHISM; FEMALE; FOOT MALFORMATION; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; HAND MALFORMATION; HUMAN; MALE; PEDIGREE; POLYDACTYLY; PRIORITY JOURNAL;

EID: 0031018457     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (60)

References (42)
  • 1
    • 0029013276 scopus 로고
    • A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination
    • Blouin J-L, Christie DH, Gos A, Lynn A, Morris MA, Ledbetter DH, Chakravarti A, et al (1995) A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. Am J Hum Genet 57:388-394
    • (1995) Am J Hum Genet , vol.57 , pp. 388-394
    • Blouin, J.-L.1    Christie, D.H.2    Gos, A.3    Lynn, A.4    Morris, M.A.5    Ledbetter, D.H.6    Chakravarti, A.7
  • 2
    • 9044249724 scopus 로고    scopus 로고
    • The t(7;11)(p15′5) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9
    • Borrow J, Shearman AM, Stanton VP Jr, Becher R, Collins T, Williams AJ, Dube I, et al (1996) The t(7;11)(p15′5) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9. Nat Genet 12:159-167
    • (1996) Nat Genet , vol.12 , pp. 159-167
    • Borrow, J.1    Shearman, A.M.2    Stanton Jr., V.P.3    Becher, R.4    Collins, T.5    Williams, A.J.6    Dube, I.7
  • 3
    • 0024212119 scopus 로고
    • Chromosomal localisation of a developmental gene in man: Direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13
    • Brueton L, Huson SM, Winter RB, Williamson R (1988) Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13. Am J Med Genet 31:799-804
    • (1988) Am J Med Genet , vol.31 , pp. 799-804
    • Brueton, L.1    Huson, S.M.2    Winter, R.B.3    Williamson, R.4
  • 7
    • 0029945149 scopus 로고    scopus 로고
    • Limbs: A model for pattern formation within the vertebrate body plan
    • Cohn MJ, Tickle C (1996) Limbs: a model for pattern formation within the vertebrate body plan. Trends Genet 12:253-257
    • (1996) Trends Genet , vol.12 , pp. 253-257
    • Cohn, M.J.1    Tickle, C.2
  • 9
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Faure, S.2    Fizames, C.3    Samson, D.4    Drouot, N.5    Vignal, A.6    Millasseau, P.7
  • 10
    • 0028004223 scopus 로고
    • How to make a limb?
    • Duboule D (1994) How to make a limb? Science 266:575-576
    • (1994) Science , vol.266 , pp. 575-576
    • Duboule, D.1
  • 11
    • 0042765264 scopus 로고
    • A note on race-specific congenital malformation rates
    • Frazier TM (1960) A note on race-specific congenital malformation rates. Am J Obstet Gynecol 80:184-185
    • (1960) Am J Obstet Gynecol , vol.80 , pp. 184-185
    • Frazier, T.M.1
  • 15
    • 0027478216 scopus 로고
    • A mouse model of Greig cephalopolysyndactyly syndrome: The extra-toes (J) mutation contains an intragenic deletion of the Gli3 gene
    • Hui C, Joyner AL (1993) A mouse model of Greig cephalopolysyndactyly syndrome: the extra-toes (J) mutation contains an intragenic deletion of the Gli3 gene. Nat Genet 3: 241-245
    • (1993) Nat Genet , vol.3 , pp. 241-245
    • Hui, C.1    Joyner, A.L.2
  • 16
    • 0024319693 scopus 로고
    • Greig syndrome in a large kindered due to reciprocal chromosomal translocation t(6;7)(q27′3)
    • Kruger G, Gotz J, Kvist U, Dunker H, Erfurth F, Pelz L, Zech L (1989) Greig syndrome in a large kindered due to reciprocal chromosomal translocation t(6;7)(q27′3). Am J Med Genet 32:411-416
    • (1989) Am J Med Genet , vol.32 , pp. 411-416
    • Kruger, G.1    Gotz, J.2    Kvist, U.3    Dunker, H.4    Erfurth, F.5    Pelz, L.6    Zech, L.7
  • 17
    • 0019492082 scopus 로고
    • An Indian family with postaxial polydactyly in four generations
    • Kucheria K, Kenue RK, Taneja N (1981) An Indian family with postaxial polydactyly in four generations. Clin Genet 20:36-39
    • (1981) Clin Genet , vol.20 , pp. 36-39
    • Kucheria, K.1    Kenue, R.K.2    Taneja, N.3
  • 19
    • 0003135726 scopus 로고
    • Phenotypic mapping in man
    • Yunis JJ (ed) Academic Press, New York
    • Lewandowski RC Jr, Yunis JJ (1977) Phenotypic mapping in man. In: Yunis JJ (ed) New chromosomal syndromes. Academic Press, New York, pp 369-394
    • (1977) New Chromosomal Syndromes , pp. 369-394
    • Lewandowski Jr., R.C.1    Yunis, J.J.2
  • 20
    • 0019352131 scopus 로고
    • A newborn infant with craniofacial dysmorphism and polysyndactyly
    • Merlob P, Grunebaum M, Reisner SH (1981) A newborn infant with craniofacial dysmorphism and polysyndactyly. Acta Pediatr Scand 70:275-277
    • (1981) Acta Pediatr Scand , vol.70 , pp. 275-277
    • Merlob, P.1    Grunebaum, M.2    Reisner, S.H.3
  • 21
    • 0014529238 scopus 로고
    • Postaxial polydactyly in three Indian families
    • Mohan J (1969) Postaxial polydactyly in three Indian families. J Med Genet 6:196-200
    • (1969) J Med Genet , vol.6 , pp. 196-200
    • Mohan, J.1
  • 22
    • 0018144776 scopus 로고
    • Autosomal recessive postaxial polydactyly type A in a Sicilian family
    • Mollica F, Li Volti S, Sorge G (1978) Autosomal recessive postaxial polydactyly type A in a Sicilian family. J Med Genet 15:212-216
    • (1978) J Med Genet , vol.15 , pp. 212-216
    • Mollica, F.1    Li Volti, S.2    Sorge, G.3
  • 23
    • 0029871929 scopus 로고    scopus 로고
    • Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
    • Muragaki Y, Mundlos S, Upton J, Olsen BR (1996) Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. Science 272:548-550
    • (1996) Science , vol.272 , pp. 548-550
    • Muragaki, Y.1    Mundlos, S.2    Upton, J.3    Olsen, B.R.4
  • 26
    • 0026774858 scopus 로고
    • A comprehensive genetic linkage map of the human genome
    • NIH/CEPH Collaborative Mapping Group (1992) A comprehensive genetic linkage map of the human genome. Science 258:67-86
    • (1992) Science , vol.258 , pp. 67-86
  • 27
    • 0008890730 scopus 로고
    • Polydactylism in related New England families
    • Odiorne JM (1943) Polydactylism in related New England families. J Hered 34:45-46
    • (1943) J Hered , vol.34 , pp. 45-46
    • Odiorne, J.M.1
  • 29
    • 0030442475 scopus 로고    scopus 로고
    • An autosomal dominant triphalangeal thumb, polysyndactyly syndrome with variable expression in a large Indian family maps to chromosome 7q36
    • Radhakrishna U, Blouin J-L, Solanki J, Dhoriani GM, Antonarakis SE (1996) An autosomal dominant triphalangeal thumb, polysyndactyly syndrome with variable expression in a large Indian family maps to chromosome 7q36. Am J Med Genet 66:209-215
    • (1996) Am J Med Genet , vol.66 , pp. 209-215
    • Radhakrishna, U.1    Blouin, J.-L.2    Solanki, J.3    Dhoriani, G.M.4    Antonarakis, S.E.5
  • 31
    • 0029127807 scopus 로고
    • Localization of the syndactly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker
    • Sarfarazi M, Akarsu AN, Sayli BS (1995) Localization of the syndactly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker. Hum Mol Genet 4:1453-1458
    • (1995) Hum Mol Genet , vol.4 , pp. 1453-1458
    • Sarfarazi, M.1    Akarsu, A.N.2    Sayli, B.S.3
  • 32
    • 0017200340 scopus 로고
    • The study of genetic variation in Nigeria. II. The genetics of polydactyly
    • Scott-Emuakpor AB, Madueke EDN (1976) The study of genetic variation in Nigeria. II. The genetics of polydactyly. Hum Hered 26:198-202
    • (1976) Hum Hered , vol.26 , pp. 198-202
    • Scott-Emuakpor, A.B.1    Madueke, E.D.N.2
  • 33
    • 0008938172 scopus 로고
    • Postaxial polydactylism in six generations of a Norwegian family
    • Sverdrup A (1922) Postaxial polydactylism in six generations of a Norwegian family. J Genet 12:217-240
    • (1922) J Genet , vol.12 , pp. 217-240
    • Sverdrup, A.1
  • 34
    • 0008926480 scopus 로고
    • Polydactyly, postaxial
    • Buyse ML (ED) Blackwell Scientific, Cambridge, MA
    • Temtamy SA (1990) Polydactyly, postaxial. In: Buyse ML (ED) Birth defects encyclopedia. Blackwell Scientific, Cambridge, MA, pp 1397-1398
    • (1990) Birth Defects Encyclopedia , pp. 1397-1398
    • Temtamy, S.A.1
  • 35
    • 0002689705 scopus 로고
    • Synopsis of hand malformation with particular emphasis on genetic factors
    • Temtamy SA, McKusick VA (1969) Synopsis of hand malformation with particular emphasis on genetic factors. Birth Defects 5:125-184
    • (1969) Birth Defects , vol.5 , pp. 125-184
    • Temtamy, S.A.1    McKusick, V.A.2
  • 36
    • 0029042877 scopus 로고
    • Report of the second international workshop on human chromosome 7 mapping
    • Tsui L-C, Donis-Keller H, Grzeschik K-H (1995) Report of the second international workshop on human chromosome 7 mapping. Cytogenet Cell Genet 71:1-30
    • (1995) Cytogenet Cell Genet , vol.71 , pp. 1-30
    • Tsui, L.-C.1    Donis-Keller, H.2    Grzeschik, K.-H.3
  • 39
    • 0026469401 scopus 로고
    • Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt)
    • Vortkamp A, Franz T, Gessler M, Grzeschik KH (1992) Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt). Mamm Genome 3:461-463
    • (1992) Mamm Genome , vol.3 , pp. 461-463
    • Vortkamp, A.1    Franz, T.2    Gessler, M.3    Grzeschik, K.H.4
  • 40
    • 0025812172 scopus 로고
    • GLI3 Zinc-finger gene interrupted by translocation in Greig syndrome families
    • Vortkamp A, Gessler M, Grzeschik K-H (1991) GLI3 Zinc-finger gene interrupted by translocation in Greig syndrome families. Nature 352:539-540
    • (1991) Nature , vol.352 , pp. 539-540
    • Vortkamp, A.1    Gessler, M.2    Grzeschik, K.-H.3
  • 41
    • 0028821386 scopus 로고
    • Isolation and characterization of a cosmid contig for the GCPS gene region
    • Vortkamp A, Heid C, Gessler M, Grzeschik KH (1995) Isolation and characterization of a cosmid contig for the GCPS gene region. Hum Genet 95:82-8
    • (1995) Hum Genet , vol.95 , pp. 82-88
    • Vortkamp, A.1    Heid, C.2    Gessler, M.3    Grzeschik, K.H.4
  • 42
    • 0344088398 scopus 로고
    • A pedigree of extra-digit-V polydactyly in a Batutsi family
    • Walker JT (1961) A pedigree of extra-digit-V polydactyly in a Batutsi family. Ann Hum Genet 25:65-68
    • (1961) Ann Hum Genet , vol.25 , pp. 65-68
    • Walker, J.T.1


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