Associated Papers
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37.
Booth KT et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findings.
Khalifa O et al.
American Journal of Medical Genetics. Part A, 2014
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