The autosomal recessive non-syndromic deafness loci, DFNB8 and DFNB10 on human chromosome 21q22.3, are distinct loci.

被引：0
|
作者：
Scott, HS
Berry, A
Korostishevsky, M
Talior, I
Barras, C
Gehrig, C
Younus, F
Veske, A
Mohyuddin, A
Mehdi, SQ
Gal, A
Kudoh, J
Shimizu, N
Bonne-Tamir, B
Antonarakis, SE
机构：
[1] Univ Geneva, Sch Med, Div Med Genet, Geneva, Switzerland
[2] Tel Aviv Univ, Sackler Sch Med, Dept Human Genet & Mol Med, IL-69978 Tel Aviv, Israel
[3] Khan Res Labs, Biomed & Genet Engn Div, Islamabad, Pakistan
[4] Univ Krankenhaus Eppendorf, Inst Humangenet, Hamburg, Germany
[5] Keio Univ, Sch Med, Dept Biol Mol, Tokyo 108, Japan
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 65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：
2523
引用
收藏
页码：A445 / A445
页数：1
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