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

页码：A445 / A445

页数：1

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