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Anuranjan AnandHemalatha BalaramManeesha InamdarUdaykumar RangaKundu Tapas K.
M. R. S. RaoKaustuv SanyalNamita SuroliaJames P. Clement ChelliahRavi Manjithaya

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  1. M. RamShankar, Aparna G, R. Jalvi, CR Srikumari Srisailapathy, V. Malhotra, S Chadha, A Agarwal, A Ramesh, R. Rangasayee and A. Anand, Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss, European Journal of Human Genetics 1 - 8 (2008).

  2. A. Kapoor, P. Satishchandra, R. Ratnapriya, Ramesh Reddy, Jayaram Kadandale, Susarla K Shankar and A. Anand, An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene, Annals of Neurology 64, 158 - 167 (2008).


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