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5. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. Hart TC; Hart PS; Gorry MC; Michalec MD; Ryu OH; Uygur C; Ozdemir D; Firatli S; Aren G; Firatli E J Med Genet; 2003 Dec; 40(12):900-6. PubMed ID: 14684688 [TBL] [Abstract][Full Text] [Related]
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12. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta. Santos MC; Hart PS; Ramaswami M; Kanno CM; Hart TC; Line SR Head Face Med; 2007 Jan; 3():8. PubMed ID: 17266769 [TBL] [Abstract][Full Text] [Related]
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