18q22.3 → 18q23 Deletion Syndrome and Cleft Palate

被引：7

作者：

Eudy, James D. ^{[3
]}

Pickering, Diane L. ^{[1
,2
]}

Lutz, Richard ^{[1
,2
]}

Platt, Kristal ^{[4
]}

Dave, Bhavana J. ^{[1
,2
]}

Olney, Ann Haskins ^{[1
,2
]}

Sanger, Warren G. ^{[1
,2
]}

机构：

[1] Univ Nebraska Med Ctr, Dept Pediat, Omaha, NE 68198 USA

[2] Univ Nebraska Med Ctr, Human Genet Lab, Munroe Meyer Inst Genet & Rehabil, Omaha, NE 68198 USA

[3] Univ Nebraska Med Ctr, Dept Genet Cell Biol & Anat, Omaha, NE 68198 USA

[4] Boys Town Natl Res Hosp, Omaha, NE 68131 USA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2010年 / 152A卷 / 04期

关键词：

CONGENITAL AURAL ATRESIA; CHROMOSOME; 18Q; PHENOTYPE;

D O I：

10.1002/ajmg.a.33336

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1046 / 1048

页数：3

共 12 条

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