Mutations in the Cx26 and CDH23 gene cause indistinguishable profound congenital hearing loss in a large Dutch family.

被引：0
|
作者：
Kremer, H
Van Hauwe, P
Hoefsloot, LH
de Brouwer, A
Pennings, R
Deutman, A
Astuto, LM
Kimberling, WJ
Bork, JM
Cremers, CWRJ
Cremers, FPM
机构：
[1] UMC Nijmegen, Dept Otorhinolaryngol, Nijmegen, Netherlands
[2] UMC Nijmegen, Dept Human Genet, Nijmegen, Netherlands
[3] UMC Nijmegen, Dept Ophthalmol, Nijmegen, Netherlands
[4] Boys Town Natl Res Hosp, Gene Marker Lab, Omaha, NE USA
[5] NIH, Lab Mol Genet, Rockville, MD USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2001年 / 69卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2394
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收藏
页码：589 / 589
页数：1
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