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25. Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome? Guazzi G; Palmeri S; Malandrini A; Ciacci G; Di Perri R; Mancini G; Messina C; Salvadori C Am J Med Genet; 1994 Mar; 50(1):79-83. PubMed ID: 8160757 [TBL] [Abstract][Full Text] [Related]
27. Demonstration of the lyon hypothesis in X-linked dominant hypoplastic amelogenesis imperfecta. Berkman MD; Singer A Birth Defects Orig Artic Ser; 1971 Jun; 7(7):204-9. PubMed ID: 5173207 [TBL] [Abstract][Full Text] [Related]
28. [A family with amelogenesis imperfecta]. Ceballos Salobreña A; Ceballos Salobreña G Av Odontoestomatol; 1988; 4(3):125-8. PubMed ID: 3252795 [No Abstract] [Full Text] [Related]
29. [A case of systemic hypomineralization of the enamel]. Hanzély B Fogorv Sz; 1971 May; 64(5):150-3. PubMed ID: 5280926 [No Abstract] [Full Text] [Related]
30. Hereditary amelogenesis imperfecta. A rare autosomal dominant type. Winter GB; Lee KW; Johnson NW Br Dent J; 1969 Aug; 127(4):157-64. PubMed ID: 5258202 [No Abstract] [Full Text] [Related]
31. A novel autosomal-recessive mutation, whitish chalk-like teeth, resembling amelogenesis imperfecta, maps to rat chromosome 14 corresponding to human 4q21. Masuyama T; Miyajima K; Ohshima H; Osawa M; Yokoi N; Oikawa T; Taniguchi K Eur J Oral Sci; 2005 Dec; 113(6):451-6. PubMed ID: 16324133 [TBL] [Abstract][Full Text] [Related]
32. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree]. De Marchi S; Proto G; Jengo A; Collinassi P; Basile A Minerva Med; 1983 Feb; 74(7):301-6. PubMed ID: 6828258 [TBL] [Abstract][Full Text] [Related]
33. [Hypo-/aplasia of the nasal bones--an autosomal dominant inherited anomaly]. Ernst M; Schilbach U HNO; 1987 Nov; 35(11):478-81. PubMed ID: 3692934 [TBL] [Abstract][Full Text] [Related]
34. Dental structural diseases mapping to human chromosome 4q21. MacDougall M Connect Tissue Res; 2003; 44 Suppl 1():285-91. PubMed ID: 12952210 [TBL] [Abstract][Full Text] [Related]
35. [A Dutch family with hereditary pancreatitis]. Lawson JA Ned Tijdschr Geneeskd; 1981 Feb; 125(8):309-12. PubMed ID: 7219588 [No Abstract] [Full Text] [Related]
36. [Clinical report on a case of amelogenesis imperfecta]. Yoshida T; Minegishi H; Osaka N; Irie E; Kurihara J; Goto H Josai Shika Daigaku Kiyo; 1981; 10(2):315-21. PubMed ID: 6959664 [No Abstract] [Full Text] [Related]