Association of deletion 22 and trisomy 21: A likely random association in patients with conotruncal heart defects

被引：5

作者：

Digilio, MC

Dallapiccola, B

Marino, B

机构：

[1] Univ Roma La Sapienza, Inst Pediat, I-00161 Rome, Italy

[2] Bambino Gesu Pediat Hosp, Rome, Italy

[3] Univ Roma La Sapienza, CSS Mendel Inst, Rome, Italy

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2005年 / 134A卷 / 01期

关键词：

D O I：

10.1002/ajmg.a.10552

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1 / 2

页数：2

共 15 条

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2-A

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[8]

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[9] Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia [J].

Digilio, MC ;

Marino, B ;

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[10]

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