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Implications in disclosing auditory genetic mutation to a family: a case study.
Int J Audiol. 2007 Jul;46(7):384-7. doi: 10.1080/14992020701297805.
Int J Audiol. 2007.
PMID: 17680470
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.
RamShankar M, Girirajan S, Dagan O, Ravi Shankar HM, Jalvi R, Rangasayee R, Avraham KB, Anand A.
RamShankar M, et al.
J Med Genet. 2003 May;40(5):e68. doi: 10.1136/jmg.40.5.e68.
J Med Genet. 2003.
PMID: 12746422
Free PMC article.
No abstract available.
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