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Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.American Journal of Human Genetics|February 24, 2015
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS lociElizabeth J Leslie, Margaret A Taub, Huan Liu, et al.American Journal of Human Genetics|March 29, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3Elizabeth J Leslie, Huan Liu, Jenna C Carlson, et al.Human Molecular Genetics|November 20, 2018
Genomic analyses in African populations identify novel risk loci for cleft palateAzeez Butali, Peter A Mossey, Wasiu L Adeyemo, et al.Pageof 7