Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
Article in Journal of Human Genetics (May 2023)
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The role of genetic factors in microtia: A systematic review
Article in F1000Research (April 2023)
Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review
Article in Molecular Genetics & Genomic Medicine (March 2023)