Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

Orofacial clefts (OFCs) are common, complex birth defects with extremely heterogeneous phenotypic presentations. Two common subtypes – cleft lip alone (CL) and cleft lip plus cleft palate (CLP) - are typically grouped into a single phenotype for genetic analysis (i.e. cleft lip with or without cleft...

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Detalhes bibliográficos
Publicado no:Genet Epidemiol
Main Authors: Carlson, Jenna C., Standley, Jennifer, Petrin, Aline, Shaffer, John R., Butali, Azeez, Buxo, Carmen J., Castilla, Eduardo, Christensen, Kaare, Deleyiannis, Frederic W-D, Hecht, Jacqueline T., Field, L. Leigh, Garidkhuu, Ariuntuul, Moreno Uribe, Lina M., Nagato, Natsume, Orioli, Ieda M., Padilla, Carmencita, Poletta, Fernando, Suzuki, Satoshi, Vieira, Alexandre R., Wehby, George L., Weinberg, Seth M., Beaty, Terri H., Feingold, Eleanor, Murray, Jeffrey C., Marazita, Mary L., Leslie, Elizabeth J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5728176/
https://ncbi.nlm.nih.gov/pubmed/29124805
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.22090
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