Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2-Reference-Cited by-同舟云学术

Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2

Published:2005 Issue:2 Volume:134A Page:158-164
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Digilio M. Cristina,Marino Bruno,Capolino Rossella,Angioni Adriano,Sarkozy Anna,Roberti M. Cristina,Conti Emanuela,de Zorzi Andrea,Dallapiccola Bruno

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference57 articles.

1. Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome

2. Tetralogy of Fallot in triplet siblings

3. 1986. Mechanisms in the pathogenesis of congenital heart defects. In: editors. The Genetics of Cardiovascular Disease. Boston, MA: Martinus-Nijoff. pp 3-11.

4. DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene

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