CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract

Juan Carlos ZentenoMaria Elena MoralesVeronica Moran-BarrosoAlejandra Sanchez-Navarro

首页> 外文期刊>Molecular vision >CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract

【24h】

CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract

机译：常染色体显性遗传性先天性白内障家庭中的CRYGD基因分析：伞形白内障分子同质性和家族内临床异质性的证据

获取原文

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Molecular vision》 |2005年第2005期|共页
作者
Juan Carlos ZentenoMaria Elena MoralesVeronica Moran-BarrosoAlejandra Sanchez-Navarro;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种
中图分类生物化学;
关键词

相似文献

外文文献
中文文献
专利

1. CRYGD gene analysis in a family with autosomal dominantcongenital cataract: evidence for molecular homogeneity andintrafamilial clinical heterogeneity in aculeiform cataract [J] . Molecular vision . 2005,第2005期

机译：常染色体显性先天性白内障家庭中的CRYGD基因分析：伞形白内障的分子同质性和家族内临床异质性的证据
2. A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity [J] . Luz M. Gonzalez-HuertaOlga M. Messina-BaasSergio A. Cuevas-Covarrubias Molecular vision . 2007,第2007期

机译：一个常染色体显性遗传性原发性白内障伴CRYGC突变的家庭：临床异质性的证据
3. A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity [J] . Luz M. Gonzalez-HuertaOlga M. Messina-BaasSergio A. Cuevas-Covarrubias Molecular vision . 2007,第2007期

机译：一个常染色体显性遗传性原发性白内障伴CRYGC突变的家庭：临床异质性的证据
4. NEXT-GENERATION ANALYSIS OF CATARACTS: DETERMINING KNOWLEDGE DRIVEN GENE-GENE INTERACTIONS USING BIOFILTER, AND GENE-ENVIRONMENT INTERACTIONS USING THE PHENX TOOLKIT [C] . SARAH A.PENDERGRASS, SHEFALI S.VERMA, MOLLY A.HALL, Pacific Symposium on Biocomputing . 2015

机译：白内障的下一代分析：使用生物过滤器确定知识驱动的基因 - 基因相互作用，以及使用Phenx工具包的基因环境相互作用
5. Genomic study and mutation functional analysis of autosomal dominant congenital cataract. [D] . Zhang, Liyun. 2007

机译：常染色体显性先天性白内障的基因组研究和突变功能分析。
6. Mutation analysis of CRYAA CRYGC and CRYGD associated with autosomal dominant congenital cataract in Brazilian families [O] . Alessandro Santana, Mauro Waiswol, Enyr Saran Arcieri, 2009

机译：巴西家庭常染色体显性先天性白内障相关的CRYAACRYGC和CRYGD突变分析
7. A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family [O] . Wang, Binbin, Yu, Changhong, Xi, Yi-Bo, 2010

机译：导致中国家庭常染色体显性先天性白内障的新型CRYGD突变（p.Trp43Arg）。

CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract

著录项

相似文献

相关主题

期刊订阅