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

页码：277 / 279

页数：3

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