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Paper Details

Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.
Genet Epidemiol
4
2019
RVs, exome, genes, linkage, multiplex cleft, oral cleft, rare variants
Author NameAffiliation
Margaret A TaubJohns Hopkins Bloomberg School of Public Health
Margaret M ParkerHarvard Medical School
Alan F ScottInstitute of Genetic Medicine, Johns Hopkins Medical Institutions
Mary L MarazitaUniversity of Pittsburgh
Ingo RuczinskiJohns Hopkins Bloomberg School of Public Health
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