Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
Based on epidemiologic and embryologic patterns, nonsyndromic orofacial clefts- the most common craniofacial birth defects in humans- are commonly categorized into cleft lip with or without cleft palate (CL/P) and cleft palate alone (CP), which are traditionally considered to be etiologically distin...
Guardado en:
Autores principales: | Debashree Ray, Sowmya Venkataraghavan, Wanying Zhang, Elizabeth J Leslie, Jacqueline B Hetmanski, Seth M Weinberg, Jeffrey C Murray, Mary L Marazita, Ingo Ruczinski, Margaret A Taub, Terri H Beaty |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/90525a7ed9d84f02a38684f2479cc4de |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting
por: Huan Liu, et al.
Publicado: (2017) -
Cytogenetic evaluation of orofacial clefts
por: Anjali Satyen Sabnis, et al.
Publicado: (2021) -
Supplementation with folic acid and orofacial clefts
por: Tovani-Palone,Marcos Roberto, et al.
Publicado: (2017) -
Prevalence of Orofacial Clefts and Associated Factors in Infants
por: S Khosroshahian, et al.
Publicado: (2021) -
Deep orofacial phenotyping of population-based infants with isolated cleft lip and isolated cleft palate
por: Mimi Yow, et al.
Publicado: (2020)