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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Pubblicato in:Genet Epidemiol
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2017
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Article
Accesso online: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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