Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate

Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a group of common human birth defects with complex etiology. Although genome-wide association studies have successfully identified a number of risk loci, these loci only account for about 20% of the heritability of orofacial clefts. The...

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Publicado no:Am J Med Genet A
Main Authors: Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Buxó, Carmen J., Castilla, Eduardo E., Christensen, Kaare, Deleyiannis, Frederic W.B., Field, L. Leigh, Hecht, Jacqueline T., Moreno, Lina, Orioli, Ieda M., Padilla, Carmencita, Vieira, Alexandre R., Wehby, George L., Feingold, Eleanor, Weinberg, Seth M., Murray, Jeffrey C., Marazita, Mary L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5444956/
https://ncbi.nlm.nih.gov/pubmed/28425186
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38210
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