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64. Palmoplantar keratosis in oculodentodigital dysplasia with a GJA1 point mutation out of the C-terminal region of connexin 43. Kogame T; Dainichi T; Shimomura Y; Tanioka M; Kabashima K; Miyachi Y J Dermatol; 2014 Dec; 41(12):1095-7. PubMed ID: 25388818 [TBL] [Abstract][Full Text] [Related]
65. Oculodentodigital syndrome: report of a case. Scheutzel P Dentomaxillofac Radiol; 1991 Aug; 20(3):175-8. PubMed ID: 1808004 [TBL] [Abstract][Full Text] [Related]
66. The G60S connexin43 mutant regulates hair growth and hair fiber morphology in a mouse model of human oculodentodigital dysplasia. Churko JM; Chan J; Shao Q; Laird DW J Invest Dermatol; 2011 Nov; 131(11):2197-204. PubMed ID: 21716323 [TBL] [Abstract][Full Text] [Related]
67. Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia. Boyden LM; Craiglow BG; Zhou J; Hu R; Loring EC; Morel KD; Lauren CT; Lifton RP; Bilguvar K; Paller AS; Choate KA J Invest Dermatol; 2015 Jun; 135(6):1540-1547. PubMed ID: 25398053 [TBL] [Abstract][Full Text] [Related]
68. Generalised hypomineralisation of enamel in oculodentodigital dysplasia: comprehensive dental management of a case. Jensen ED BMJ Case Rep; 2021 Jan; 14(1):. PubMed ID: 33431460 [TBL] [Abstract][Full Text] [Related]
69. [Hair dysplasia in oculo-dento-digital syndrome. Apropos of a mother-daughter case]. Adamski H; Chevrant-Breton J; Odent S; Patoux-Pibouin M; Le Marec B; Laudren A; Urvoy M Ann Dermatol Venereol; 1994; 121(10):694-9. PubMed ID: 7793757 [TBL] [Abstract][Full Text] [Related]
71. Complex toe syndactyly with characteristic facial phenotype: a new syndrome? Sobreira NL; Cernach MC; Brunoni D; Perez AB Am J Med Genet A; 2008 Jul; 146A(13):1725-8. PubMed ID: 18512233 [TBL] [Abstract][Full Text] [Related]
73. Cardiac arrhythmia and death of teenager linked to rare genetic disorder diagnosed at autopsy. Quick JS; Dobersen M Am J Forensic Med Pathol; 2014 Jun; 35(2):103-5. PubMed ID: 24781393 [TBL] [Abstract][Full Text] [Related]
74. Dental management of oculodentodigital dysplasia: report of case. Dean JA; Jones JE; Vash BW ASDC J Dent Child; 1986; 53(2):131-4. PubMed ID: 2937820 [TBL] [Abstract][Full Text] [Related]
75. OCULO-DENTO-DIGITAL DYSPLASIA IN A TUNISIAN FAMILY WITH A NOVEL GJA1 MUTATION. Attig A; Trabelsi M; Hizem S; Ben Jemaa L; Maazoul F; Chaouachi S; Mrad R Genet Couns; 2016; 27(3):433-439. PubMed ID: 30204976 [No Abstract] [Full Text] [Related]
76. Clinical manifestations of oculodentodigital dysplasia. Kayalvizhi G; Subramaniyan B; Suganya G J Indian Soc Pedod Prev Dent; 2014; 32(4):350-2. PubMed ID: 25231047 [TBL] [Abstract][Full Text] [Related]
77. A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome. Richardson RJ; Joss S; Tomkin S; Ahmed M; Sheridan E; Dixon MJ J Med Genet; 2006 Jul; 43(7):e37. PubMed ID: 16816024 [TBL] [Abstract][Full Text] [Related]
78. Ectopic acanthosis nigricans occurring in a child after syndactyly repair. Wu JC; Cunningham BB Cutis; 2008 Jan; 81(1):22-4. PubMed ID: 18306842 [TBL] [Abstract][Full Text] [Related]
79. [Two new cases of the oculo-dento-digital syndrome (author's transl)]. Levai JP; Cisterne JP; Malpuech G; Fourrier P Sem Hop; 1980 May 18-25; 56(19-20):992-3. PubMed ID: 6251567 [TBL] [Abstract][Full Text] [Related]
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