Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects

Despite considerable advances in the detection of genomic abnormalities in congenital heart disease (CHD), the etiology of CHD remains largely unknown. CHD is the most common birth defect and is a major cause of infant morbidity and mortality, and conotruncal defects constitute 20% of all CHD cases....

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Detalles Bibliográficos
Autores principales: de Souza, Karen Regina, Mergener, Rafaella, Huber, Janaina, Campos Pellanda, Lucia, Riegel, Mariluce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475533/
https://www.ncbi.nlm.nih.gov/pubmed/26137477
http://dx.doi.org/10.1155/2015/401941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475533/
https://www.ncbi.nlm.nih.gov/pubmed/26137477
http://dx.doi.org/10.1155/2015/401941

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