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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306129/
https://www.ncbi.nlm.nih.gov/pubmed/34356046
http://dx.doi.org/10.3390/genes12071030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306129/
https://www.ncbi.nlm.nih.gov/pubmed/34356046
http://dx.doi.org/10.3390/genes12071030

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