22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil-Reference-Cited by-同舟云学术

22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil

Published:2008-07-01 Issue:13 Volume:146A Page:1655-1661
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Rosa Rafael F.M.,Pilla Carlo B.,Pereira Vera L.B.,Flores José A.M.,Golendziner Eliete,Koshiyama Dayane B.,Hertz Michele T.,Ricachinevsky Cláudia P.,Roman Tatiana,Varella‐Garcia Marileila,Paskulin Giorgio A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference39 articles.

1. American Journal of Medical Genetics 01487299 10968628 2004

2. Major congenital heart disease in Northern Norway: Shortcomings of pre‐ and postnatal diagnosis;Acharya;Acta Obstet Gynecol Scand,2004

3. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot;Amati;Hum Genet,1995

4. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: No evidence for deletions in non‐syndromic patients;Borgmann;Eur J Pediatr,1999

5. Racial and temporal variations in the prevalence of heart defects;Botto;Pediatrics,2001

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