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Paper Details

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
Am J Hum Genet
122
2016
CP, Cleft palate, GRHL3, Nonsyndromic Cleft Palate, Thr454Met, birth defect, infants, luciferase, nonsyndromic CP, nonsyndromic orofacial clefting, physical and cognitive disabilities, rs41268753, wild-type GRHL3, zebrafish
Author NameAffiliation
Deepti JainUniversity of Washington
Cathy C LaurieUniversity of Washington
Kimberly F DohenyCenter for Inherited Disease Research, Johns Hopkins University
Toby McHenryCenter for Craniofacial and Dental Genetics, University of Pittsburgh
Robert A CornellUniversity of Iowa
Robert A CornellUniversity of Iowa
Mary L MarazitaCenter for Craniofacial and Dental Genetics, University of Pittsburgh, Graduate School of Public Health, USA Clinical and Translational Science
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