Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
Hart PS; Becerik S; Cogulu D; Emingil G; Ozdemir-Ozenen D; Han ST; Sulima PP; Firatli E; Hart TC; Clinical Genetics, 2009, vol. 75, issue 4, p 401, ISSN 13990004. ISBN 13990004.

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