Chromosome 1q deletion and congenital glaucoma

被引：3
|
作者：
Okamoto, N
Hatsukawa, Y
Shiraishi, J
Harada, N
Matsumoto, N
机构：
[1] Osaka Med Ctr, Dept Planning & Res, Osaka 5941101, Japan
[2] Res Inst Maternal & Child Hlth, Osaka 5941101, Japan
[3] Osaka Med Ctr, Dept Ophthalmol, Osaka 5941101, Japan
[4] Osaka Med Ctr, Dept Neonatol Med, Osaka 5941101, Japan
[5] Res Inst Maternal & Child Hlth, Osaka, Japan
[6] Nagasaki Univ, Grad Sch Biomed Sci, Dept Human Genet, Nagasaki 852, Japan
[7] Kyushu Med Sci Nagasaki Lab, Nagasaki, Japan
[8] Japan Sci & Technol Corp, CREST, Kawaguchi, Japan
[9] Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
来源：
PEDIATRICS INTERNATIONAL | 2005年 / 47卷 / 04期
关键词：
antithrombin-III; congenital glaucoma; gain of function; haploinsufficiency; interstitial 1q deletion syndrome; MYOC gene;
D O I：
10.1111/j.1442-200x.2005.02097.x
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
[No abstract available]
引用
收藏
页码：477 / 479
页数：3
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