Associated Papers
Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.
Downie L et al.
European Journal of Human Genetics : Ejhg, 2020
The Clinical Next-Generation Sequencing Database: A Tool for the Unified Management of Clinical Information and Genetic Variants to Accelerate Variant Pathogenicity Classification.
Nishio SY et al.
Human Mutation, 2017
28008688 (PubMed )
Supplement: HUMU-38-252-s001.pdf
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