Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States

Conotruncal defects with normally related great vessels (CTD-NRGVs) occur in both patients with and without 22q11.2 deletion syndrome (22q11.2DS), but it is unclear to what extent the genetically complex etiologies of these heart defects may overlap across these two groups, potentially involving var...

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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: Oluwafemi, Omobola O., Musfee, Fadi I., Mitchell, Laura E., Goldmuntz, Elizabeth, Xie, Hongbo M., Hakonarson, Hakon, Morrow, Bernice E., Guo, Tingwei, Taylor, Deanne M., McDonald-McGinn, Donna M., Emanuel, Beverly S., Agopian, A. J.
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8306129/
https://ncbi.nlm.nih.gov/pubmed/34356046
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12071030
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