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Dive into the research topics of 'Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.'. Together they form a unique fingerprint.- Sort by
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M. RamShankar, S. Girirajan, O. Dagan, H. M. Ravi Shankar, R. Jalvi, R. Rangasayee, K. B. Avraham, A. Anand
Research output: Contribution to journal › Article › peer-review