Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3

被引：35
作者：
Haberlandt, E
Löffler, J
Hirst-Stadlmann, A
Stöckl, B
Judmaier, W
Fischer, H
Heinz-Erian, P
Müller, T
Utermann, G
Smith, RJH
Janecke, AR
机构：
[1] Univ Innsbruck, Inst Med Biol & Human Genet, A-6020 Innsbruck, Austria
[2] Univ Innsbruck Hosp, Dept Paediat, A-6020 Innsbruck, Austria
[3] Univ Innsbruck Hosp, Dept Hearing, A-6020 Innsbruck, Austria
[4] Univ Innsbruck Hosp, Dept Speech, A-6020 Innsbruck, Austria
[5] Univ Innsbruck Hosp, Dept Voice Disorders ENT, A-6020 Innsbruck, Austria
[6] Univ Innsbruck Hosp, Dept Orthopaed, A-6020 Innsbruck, Austria
[7] Univ Innsbruck Hosp, Inst MR Imaging & Spect, A-6020 Innsbruck, Austria
[8] Univ Iowa Hosp & Clin, Dept Otolaryngol, Iowa City, IA 52242 USA
来源：
JOURNAL OF MEDICAL GENETICS | 2001年 / 38卷 / 06期
关键词：
D O I：
10.1136/jmg.38.6.405
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：405 / 409
页数：5
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