Hypogammaglobulinemia and Silver-Russell Phenotype Associated With Partial Trisomy 7q and Partial Monosomy 21q

被引：3
|
作者：
Artac, Hasibe [1 ]
Reisli, Ismail [1 ]
Yildirim, Mahmut Selman [2 ]
Bagci, Gulseren [3 ]
Luleci, Guven [3 ]
Hosgor, Orhan [4 ]
Karaaslan, Sevim [5 ]
机构：
[1] Selcuk Univ, Meram Med Fac, Dept Pediat, Div Immunol & Allergy, TR-42080 Beysehir Yolu, Konya, Turkey
[2] Selcuk Univ, Meram Med Fac, Dept Genet, TR-42080 Beysehir Yolu, Konya, Turkey
[3] Akdeniz Univ, Fac Med, Dept Genet, TR-07058 Antalya, Turkey
[4] Antalya Govt Hosp, Dept Obstet & Gynecol, Antalya, Turkey
[5] Selcuk Univ, Meram Med Fac, Dept Pediat, Div Cardiol, TR-42080 Beysehir Yolu, Konya, Turkey
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2009年 / 149A卷 / 02期
关键词：
PRENATAL-DIAGNOSIS; CHROMOSOME-21; DELETION;
D O I：
10.1002/ajmg.a.32617
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：277 / 279
页数：3
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