Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175 (vol 5, pg 169, 1996)

被引：0

|

作者：

Brown, KA

Janjua, AH

Karbani, G

Parry, G

Noble, A

Crockford, G

Bishop, DT

Newton, VE

Markham, AF

Mueller, RF

机构：

来源：

HUMAN MOLECULAR GENETICS | 1996年 / 5卷 / 05期

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

收藏

页码：710 / 710

页数：1

相关论文

共 2 条

[1] Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175
Brown, KA
Janjua, AH
Karbani, G
Parry, G
Noble, A
Crockford, G
Bishop, DT
Newton, VE
Markham, AF
Mueller, RF
HUMAN MOLECULAR GENETICS, 1996, 5 (01) : 169 - 173
[2] Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran:: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness
Esmaeili, Mohsen
Bonyadi, Mortaza
Nejadkazem, Mohammad
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2007, 71 (06) : 869 - 873