Rare genetic variants in SEC24D modify orofacial cleft phenotypes

As one of the most common structural birth defects, orofacial clefts (OFCs) have been studied for decades, and recent studies have demonstrated that there are genetic differences between the different phenotypic presentations of OFCs. However, the contribution of rare genetic variation genome-wide t...

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Detalles Bibliográficos
Autores principales: Curtis, Sarah W., Carlson, Jenna C., Beaty, Terri H., Murray, Jeffrey C., Weinberg, Seth M., Marazita, Mary L., Cotney, Justin L., Cutler, David J., Epstein, Michael P., Leslie, Elizabeth J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081436/
https://www.ncbi.nlm.nih.gov/pubmed/37034635
http://dx.doi.org/10.1101/2023.03.24.23287714

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081436/
https://www.ncbi.nlm.nih.gov/pubmed/37034635
http://dx.doi.org/10.1101/2023.03.24.23287714

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