Associated Papers
High-frequency actionable pathogenic exome variants in an average-risk cohort.
Rego S et al.
Cold Spring Harbor Molecular Case Studies, 2018
30487145 (PubMed )
Supplement: supp_mcs.a003178_Supplemental_File_1.xlsx › Sheet1
Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing.
Leone MP et al.
Molecular and Cellular Probes, 2017
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