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Paper Details

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.
Am J Hum Genet
44
2020
OFC, OFC syndromes, OFCs, Orofacial Cleft, SOX2, SOX2-interacting genes, birth defects, coding DNMs, congenital defects, human, orofacial clefts, zinc
Author NameAffiliation
Margaret A TaubBloomberg School of Public Health, Johns Hopkins University
Ingo RuczinskiBloomberg School of Public Health, Johns Hopkins University
David J CutlerEmory University School of Medicine
David J CutlerEmory University School of Medicine
Mary L MarazitaUniversity of Pittsburgh School of Dental Medicine, University of Pittsburgh Graduate School of Public Health
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Release 1.2