Identification of a novel gene causing the pleiotropic features of Nance-Horan Syndrome.

被引：0
|
作者：
Burdon, KP
McKay, JD
Sale, MM
Russell-Eggitt, IM
Mackey, DA
Wirth, MG
FitzGerald, LM
Shaw, M
Sharma, S
Gajovic, S
Gruss, P
Ross, S
Thomas, P
Voss, AK
Thomas, T
Gécz, J
Craig, JE
机构：
[1] Univ Tasmania, Menzies Ctr Populat Hlth Res, Hobart, Tas, Australia
[2] Wake Forest Univ, Sch Med, Ctr Human Genom, Winston Salem, NC USA
[3] Great Ormond St Hosp Children, London WC1N 3JH, England
[4] Univ Melbourne, Royal Victorian Eye & Ear Hosp, Ctr Eye Res Australia, Melbourne, Vic, Australia
[5] Womens & Childrens Hosp, Dept Cytogenet & Mol Genet, Adelaide, SA, Australia
[6] Flinders Univ S Australia, Dept Ophthalmol, Bedford Pk, SA 5042, Australia
[7] Max Planck Inst Biophys Chem, Dept Mol Cell Biol, Gottingen, Germany
[8] Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[9] Walter & Eliza Hall Inst Med Res, Parkville, Vic, Australia
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05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：
35
引用
收藏
页码：169 / 169
页数：1
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