Publications
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Filters: Author is Scharpf, Robert B [Clear All Filters]
, “Detection of rare disease variants in extended pedigrees using RVS.”, Bioinformatics, 2018.
, “Whole exome association of rare deletions in multiplex oral cleft families.”, Genet Epidemiol, vol. 41, no. 1, pp. 61-69, 2017.
