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American Journal of Bioethics, Vol. 13, Iss. 10, 2013-10 ,pp. : 61-61

Routledge Ltd

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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

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Oxford University Press

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Distal 7q11.23 Duplication, an Emerging Microduplication Syndrome: A Case Report and Further Characterisation

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A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness ( DFNA11 ) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene

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Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

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