Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes

Nonsyndromic orofacial clefts (OFCs) are among the most common craniofacial birth defects worldwide, and known to exhibit phenotypic and genetic heterogeneity. Cleft lip plus cleft palate (CLP) and cleft lip only (CL) are commonly combined together as one phenotype (CL/P), separately from cleft pala...

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Veröffentlicht in:	Genetic epidemiology 2022-04, Vol.46 (3-4), p.182-198
Hauptverfasser:	Mukhopadhyay, Nandita, Feingold, Eleanor, Moreno‐Uribe, Lina, Wehby, George, Valencia‐Ramirez, Luz Consuelo, Restrepo Muñeton, Claudia P., Padilla, Carmencita, Deleyiannis, Frederic, Christensen, Kaare, Poletta, Fernando A., Orioli, Ieda M., Hecht, Jacqueline T., Buxó, Carmen J., Butali, Azeez, Adeyemo, Wasiu L., Vieira, Alexandre R., Shaffer, John R., Murray, Jeffrey C., Weinberg, Seth M., Leslie, Elizabeth J., Marazita, Mary L.
Format:	Artikel
Sprache:	eng
Schlagworte:	Birth defects Brain - abnormalities Cleft Lip - genetics Cleft lip/palate Cleft Palate - genetics comparison of genetic etiology Congenital defects DNA-Binding Proteins - genetics Genome-Wide Association Study Genomes genome‐wide association Humans Interferon Regulatory Factors - genetics multiethnic study Netrin-1 Orofacial clefts Phenotype Phenotypes Polymorphism, Single Nucleotide Single-nucleotide polymorphism subtypes of orofacial clefts
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