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Paper Details

Whole exome association of rare deletions in multiplex oral cleft families.
Genet Epidemiol
8
2017
SNVs, coding DNA, coding regions, eight regions, exomes, genome, hemizygous deletions, nonsyndromic clefts, nonsyndromic oral cleft, oral cleft, rare deletions, rare hemizygous deletions, rare sequence variants
Author NameAffiliation
Alan F ScottCenter for Inherited Disease Research, Johns Hopkins School of Medicine
Alan F ScottInstitute of Genetic Medicine, Johns Hopkins School of Medicine
Margaret M ParkerBrigham and Women's Hospital
Mary L MarazitaCenter for Craniofacial and Dental Genetics, University of Pittsburgh
Ingo RuczinskiJohns Hopkins Bloomberg School of Public Health
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