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复杂的家族性多指并指2例矫治成功报告

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出处 《实用手外科杂志》 2005年第1期62-63,F004,共3页 Journal of Practical Hand Surgery
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参考文献10

  • 1Goodman FR, Mundlos S, Muragaki Y, Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract[M]. Proc Natl Acad Sci,1997,94(14):7458-7463.
  • 2Tsukurov O, Boehmer A, Flynn J. A complex bilateral polysyndactyly disease locus maps to chromosome7q36[J]Nat Genet,1994,6(3):282-286.
  • 3Vortamp A, Gessler M, Grzeschik KH,et al. GLI3 zine-finger gene interrupted by translocation in Greig syndrome families[J]. Nature, 1991, 352(6335):539-540
  • 4Gladwin A, Donnai D,Metcalfe K, et al. Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24[J]. Hum Molec Genet, 1997,6:123-127.
  • 5Radhakrishna U, Blouin JL, Mehenni H, et al Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11. 23 by linkage analysis[J]. Am J Hum Genet, 1997,60(3):597-604.
  • 6Rogers JF. Clinical delineation of proximal and distal partial 13q trisomy[J].Clin Genet, 1984, 25(3):221-229.
  • 7Bosse K, Betz RC, Lee YA, Localization of a gene for syndactyiy type 1 to chromosome 2q34-q36[J]. Am J Hum Genet, 2000,67(2):492-497.
  • 8赵红珊,黄尚志,邹颖,柴精华,李辉,李明月.多指(趾)家系疾病相关基因排除性定位分析[J].中华医学遗传学杂志,2000,17(1):6-9. 被引量:7
  • 9秦炜,舒安利,邢清和,秧茂盛,冯国鄞,贺林.一先天性并指中国家系的遗传学研究[J].Acta Genetica Sinica,2003,30(10):973-977. 被引量:5
  • 10Zhao H, Tian Y, Breedveld G, et al. Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13.1-13.2 in a Chinese kindred[J].Eur J Hum Genet,2002,10(3):162-166.

二级参考文献27

  • 1郑之怀,阙正龙,郭勇.注射氰化物中毒死亡1例[J].中国法医学杂志,2004,19(6):373-374. 被引量:4
  • 2Temtamy S A, McKusick V A. Syndactyly as an isolated malformation. In : The genetics of hand malformations. Birth defects : original article series vol. XIV(3). New York:Alan R. Liss, 1978,301~322.
  • 3Bosse K, Betz R C, Lee Y A, Wienker T F, Reis A, Kleen H, Propping P, Cichon S, Nothen M M. Localization of a gene for syndactyly type 1 to chromosome 2q34-q36. Am J Hum Genet, 2000, 67 : 492~497.
  • 4Sarfarazi M, Akarsu A N, Sayli B S. Localization of the syndactyly type Ⅱ (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker. Hum Molec Genet , 1995,4:1453~1458.
  • 5Gladwin A, Donnai D, Metcalfe K, Schrander-Stumpel C, Brueton L,Verloes A, Aylsworth A, Toriello H, Winter R, Dixon, M. Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24. Hum Molec Genet, 1997,6:123~127.
  • 6Akarsu A N, Stoilov I, Yilmaz E, Sayli B S, Sarfarazi M. Genomic structure of HOXDI3 gene:a nine polyalanine duplication causes synpolydactyly in two unrelated families. Hum Mol Genet, 1996,5:945~952.
  • 7Bo Gao, Jingzhi Guo, Chaowen She, Anli Shu, Maosheng Yang, Zheng Tan, Xinping Yang, Shengzhen Guo, Guoying Fang, Lin He. Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1.Nature Genet,2001,28:386~388.
  • 8Xinping Yang, Chaowen She, Jingzhi Guo, Albert CH Yu, Yingjin Lu,XiaoLiu Shi, Guoying Feng, Lin He. A Locus for Brachydactyly Type A-1 Maps to Chromosome 2q35-q36. Am J Hum Genet, 2000, 66:892~903.
  • 9Thomsen O. Einige Eigentuemlichkeiten der erblichen Poly-und Syndaktylie bei Menschen. Acta Med Scand, 1927,65:609~644.
  • 10Alvord R M. Zygodactyly and associated variations in a Utah family. J Hered, 1947,38:49~53.

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