Rapid umbilical cord diagnostic of hereditary profound hearing loss: how we do it

被引：1

作者：

Birkenhaeger, R. ^{[1
]}

Maier, W. ^{[1
]}

Kunze, M. ^{[2
,3
]}

Aschendorff, A. ^{[1
]}

Arndt, S. ^{[1
]}

机构：

[1] Univ Med Ctr Freiburg, Dept Oto Rhino Laryngol Head & Neck Surg, D-79106 Freiburg, Germany

[2] Univ Med Ctr Freiburg, Dept Gynecol, D-79106 Freiburg, Germany

[3] Univ Med Ctr Freiburg, Dept Obstet, D-79106 Freiburg, Germany

来源：

CLINICAL OTOLARYNGOLOGY | 2009年 / 34卷 / 04期

关键词：

GENOTYPE-PHENOTYPE CORRELATION; PENDRED-SYNDROME; MUTATIONS; DEAFNESS; GENE;

D O I：

10.1111/j.1749-4486.2009.01958.x

中图分类号：

R76 [耳鼻咽喉科学];

学科分类号：

100213 ;

摘要：

引用

页码：374 / 376

页数：3

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