常染色体显性遗传性聋大家系的遗传学特征分析
Clinical Genetics Investigation in Two Large Chinese Kindreds with Autosomal Dominant Hereditary Non-syndromic Hearing Loss
纵亮;王秋菊;兰兰;袁虎;郭维维;韩东一;
1:解放军总医院耳鼻咽喉-头颈外科
2:解放军总医院耳鼻咽喉-头颈外科
3:解放军总医院耳鼻咽喉-头颈外科
4:解放军总医院耳鼻咽喉-头颈外科
摘要关键词基金项目(Foundation):作者参考文献1 Adato A,Raskin L,Petit C,et al.Deafness heterogeneltyin a Druze isolate fromthe Middl East:novel OTOF and PDS mutations,low prevalence of GJB23SdelG mutationandindicationfor a newDFNBlo-cus[J].Eur HumGenet,2000,8:437.
2 王秋菊,杨伟炎,方跃云,等.常染色体显性遗传性耳聋家系的遗传学特征分析[J].中国听力语言康复科学杂志,2003,1:18.
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