22q11.2 deletion syndrome and complex congenital heart defects
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Publisher
Elsevier BV
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 Medicine, Johns Hopkins University and National Center for Biotechnology 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 avaliação clínica e técnica de FISH;Koshiyama;Rev Assoc Med Bras,2009
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