Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

被引：53
|
作者：
Yatsenko, SA
Cheung, SW
Scott, DA
Nowaczyk, MJM
Tarnopolsky, M
Naidu, S
Bibat, G
Patel, A
Leroy, JG
Scaglia, F
Stankiewicz, P
Lupski, JR
机构：
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Houston, TX 77030 USA
[4] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON, Canada
[5] McMaster Univ, Dept Med, Hamilton, ON, Canada
[6] McMaster Univ, Dept Pediat, Hamilton, ON, Canada
[7] Johns Hopkins Univ, Baltimore, MD USA
[8] Kennedy Krieger Inst, Baltimore, MD USA
[9] State Univ Ghent Hosp, Dept Med Genet, B-9000 Ghent, Belgium
来源：
JOURNAL OF MEDICAL GENETICS | 2005年 / 42卷 / 04期
关键词：
D O I：
10.1136/jmg.2004.028258
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页码：328 / 335
页数：8
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