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先天性白内障的研究进展 被引量:1

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出处 《中国优生与遗传杂志》 2006年第9期129-129,94,共2页 Chinese Journal of Birth Health & Heredity
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  • 1Bhatti TR,Dott M,Yoon PW,et al. Descriptive epidemiology of infantile cataracts in metropolitan Atlanta, GA,1968- 1998[J]. Arch Pediatr Adolesc Med, 2003, 157(4) :341 - 347.
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  • 6M.I. Rees,P. Watts,I. Fenton,A. Clarke,R.G. Snell,M.J. Owen,J. Gray.Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3)[J]. Human Genetics . 2000 (2)
  • 7Vanita Berry,Donna Mackay,Shagufta Khaliq,Peter J. Francis,Abdul Hameed,Khalid Anwar,S. Qasim Mehdi,Richard J. Newbold,Alex Ionides,Alan Shiels,Tony Moore,Shomi S. Bhattacharya.Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin[J]. Human Genetics . 1999 (1-2)
  • 8Hans Eiberg,Allan Meldgaard Lund,Mette Warburg,Thomas Rosenberg.Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36[J]. Human Genetics . 1995 (1)
  • 9ShielsA,MackayD,IonidesA ,etal.Amissensemutationinthehumanconnexin50gene (GJA8)underliesautosomaldominant"zonularpulverulent"cataract,onchromosome1q. AmJHumGenet . 1998
  • 10Vanita SinghJR,SarhadiVK ,etal.Anovelformof"centralpouchlike"cataract,withsuturalopacities,mapstochromosome15 q2122. AmJHumGenet . 2001

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