期刊文献+

遗传性先天性白内障伴高度近视一家系

下载PDF
导出
出处 《眼科研究》 CSCD 北大核心 2009年第2期125-126,共2页 Chinese Ophthalmic Research
基金 天津市应用基础及前沿技术研究计划项目资助(08JCYBJC08600)
  • 相关文献

参考文献8

  • 1Ionides A, Francis P, Berry V, et al. Clinical and genetic heterogenity in autosomal dominant cataract[ J ]. Br J Ophthahnol, 1999 83 : 802 - 808
  • 2Edwards M, Lewis WH. Autosomal recessive inheritance of myopia in Hong Kong Chinese infants [ J ]. Ophthalmic Physiol Opt, 1991 , 11 : 227 - 231
  • 3Reddy MA,Francis PJ,Berry V, et al. Molecular genetic basis of inherited cataract and associated phenotypes [ J ]. Surv Ophthahnol, 2004, 49 : 300 -315
  • 4Sun H, Ma Z, Li Y, et al. Gamma-Scrystallin gene (CRYGS) mutation causes dominant progressive cortical cataract in humans[ J]. J Med Genet, 2006,42: 706 - 710
  • 5Gao L, Qin W, Cui H, et al. A novel locus of eoralliform cataractmapped to chromosome 2p24- pter [J]. J Hum Genet, 2005, 50: 305 - 310
  • 6Guggenheim JA, Kirov G, Hodson SA. The heritability of high myopia : reanalysis of Goldschmidt' s data[J]. J Med Genet,2000,37(3):227-231
  • 7陆宏,孙慧敏.高度近视遗传学和基因定位研究进展[J].眼科新进展,2006,26(6):462-465. 被引量:14
  • 8Naiglin L, Gazagne C, Dallongeville F, et al. A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36 [ J ]. J Med Genet,2002,39:118 - 124

二级参考文献24

  • 1Young TL, Ronan SM, Drahozal LA, Wildenberg SC,Alvear AB,Oetting WS, et al.Evidence that a locus for familial high myopia maps to chromosome 18p[J]. Am J Hum Genet 1998; 63(1): 109-119.
  • 2Wong T. Y,Foster PJ,Hee J,Ng TP,Tielsch JM,Chew SJ,et al. Prevalence and risk factors for refractive errors in adult Chinese in Singapore [J]. Invest Ophthalmol Vis Sci 2000;41(9):2486-2494.
  • 3Olmedo MV, Munoz JI, Rodriguez-Cid MJ, Carracedo A,Gomez-Ulla FJ, Salorio MS. Two different genetic markers for high and low myopia[J]. Eur J Ophthalmol 1992;2(4): 196-199.
  • 4Gwiazda J, Thorn F, Bauer J, Held R. Myopic children show insufficient accommodative response to blur [J].Invest Ophthalmol Vis Sci 1993;34(3):690-694.
  • 5Guggenheim JA,Kirov G, Hodson SA. The heritability of high myopia: a reanalysis of Goldschmidt's data [J]. J Med Genet 2000;37(3):227-231.
  • 6Lyhne N, Sjolie AK, Kyvik KO, Green A. The importance of genes and environment for ocular refraction and its determiners:a population based study among 20-45 year old twins[J].Br J Ophthalmol 2001;85(12): 1470-1476.
  • 7Hammond CJ, Snieder H, Gilbert CE, Spector TD. Genes and environment in refractive error: the twin eye study[J]. Invest Ophthalmol Vis Sci 2001;42(6): 1232-1236.
  • 8Hammond CJ, Andrew T, Mak YT, Spector TD. A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twins[J]. Am J Hum Gnet 2004; 75 (2): 294-304.
  • 9Morton NE,MacLean CJ, Lew R, Yee S. Multipoint linkage analysis[J].Am J Hum Genet 1986;38(6):868-883.
  • 10Schwartz M, Haim M, Skarsholm D. X-linked myopia:Bornholm eye disease. Linkage to DNA markers on the distal part of Xq[J]. Clin Genet 1990;38(4) :281-286.

共引文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部