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35. Hereditary and idiopathic anomalies of tooth number, structure and form. Winter GB Dent Clin North Am; 1969 Apr; 13(2):355-73. PubMed ID: 5251329 [No Abstract] [Full Text] [Related]
36. A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndrome. Jalili IK; Smith NJ J Med Genet; 1988 Nov; 25(11):738-40. PubMed ID: 3236352 [TBL] [Abstract][Full Text] [Related]
37. [An enamel disorder in two siblings]. Créton MA; Cune MS Ned Tijdschr Tandheelkd; 2004 Oct; 111(10):400-2. PubMed ID: 15553370 [TBL] [Abstract][Full Text] [Related]
39. Amelogenesis imperfecta in a new animal model--a mutation in chromosome 5 (human 4q21). Seedorf H; Springer IN; Grundner-Culemann E; Albers HK; Reis A; Fuchs H; Hrabe de Angelis M; Açil Y J Dent Res; 2004 Aug; 83(8):608-12. PubMed ID: 15271968 [TBL] [Abstract][Full Text] [Related]
40. Restoring function and esthetics in a patient with amelogenesis imperfecta: a case report. Sengun A; Ozer F Quintessence Int; 2002 Mar; 33(3):199-204. PubMed ID: 11921768 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]