Chromosomal abnormalities among children born with conotruncal cardiac defects

BACKGROUND: Conotruncal heart defects comprise 25%-30% of non-syndromic congenital heart defects. This study describes the frequency of chromosome abnormalities and microdeletion 22q11 associated with conotruncal heart malformations. METHODS: From a population base of 974,579 infants/fetuses deliver...

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Bibliografiset tiedot
Päätekijät: Lammer, Edward J., Chak, Jacqueline S., Iovannisci, David M., Schultz, Kathleen, Osoegawa, Kazutoyo, Yang, Wei, Carmichael, Suzan L., Shaw, Gary M.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2856481/
https://ncbi.nlm.nih.gov/pubmed/19067405
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.20541
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