Síndrome de deleção 22q11 e cardiopatias congênitas complexas-Reference-Cited by-同舟云学术

Síndrome de deleção 22q11 e cardiopatias congênitas complexas

Published:2011-01 Issue:1 Volume:57 Page:62-65
ISSN:0104-4230
Container-title:Revista da Associação Médica Brasileira
language:pt
Short-container-title:Revista da Associação Médica Brasileira

Author:

Machado Rosa Rafael Fabiano,Trevisan Patrícia,Koshiyama Dayane Bohn,Pilla Carlo Benatti,Gazzola Zen Paulo Ricardo,Varella-Garcia Marileila,Paskulin Giorgio Adriano

Publisher

Elsevier BV

Subject

General Medicine

Link

http://www.scielo.br/pdf/ramb/v57n1/en_v57n1a18.pdf

Reference20 articles.

1. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies;Iserin;Eur J Pediatr.,1998

2. Online Mendelian Inheritance in Man, OMIM (TM). [cited 2010 sept 30]. Bethesda: BeMcKusick-Nathans Institute for Genetic Medi cine, Johns Hopkins University and National Center for Biotechnol ogy Information, National Library of Medicine; 2000. Disponível em: http://www.ncbi.nlm.nih.gov/omim/.

3. 22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil;Rosa;Am J Med Genet.,2008

4. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery;Ziolkowska;Eur J Pediatr.,2008

5. Síndrome de deleção 22q11.2: importância da aval iação clínica e técnica de FISH;Koshiyama;Rev Assoc Med Bras.,2009

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1. Investigação Citogenômica de Crianças com Doença Cardíaca Congênita: Experiência de um Centro no Brasil;Arquivos Brasileiros de Cardiologia;2021-11-17

2. The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review;Journal of Pediatric Genetics;2019-10-23

3. A novel TBX1 missense mutation in patients with syndromic congenital heart defects;Biochemical and Biophysical Research Communications;2018-05

4. Congenital Heart Disease as a Warning Sign for the Diagnosis of the 22q11.2 Deletion;Arquivos Brasileiros de Cardiologia;2014