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24. Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 gene. van Es RJ; Wittebol-Post D; Beemer FA Int J Oral Maxillofac Surg; 2007 Sep; 36(9):858-60. PubMed ID: 17509830 [TBL] [Abstract][Full Text] [Related]
25. Oculodentodigital Dysplasia with a Novel Mutation in Choi J; Yang A; Song A; Lim M; Kim J; Jang JH; Park KT; Cho S; Jin DK Ann Clin Lab Sci; 2018 Nov; 48(6):776-781. PubMed ID: 30610049 [TBL] [Abstract][Full Text] [Related]
26. Oculodentodigital dysplasia with cerebral white matter abnormalities in a two-generation family. Norton KK; Carey JC; Gutmann DH Am J Med Genet; 1995 Jul; 57(3):458-61. PubMed ID: 7677152 [TBL] [Abstract][Full Text] [Related]
27. Orodigitofacial dysostosis and oculodentodigital dysplasia. Two distinct syndromes with some similarities. Eidelman E; Chosack A; Wagner ML Oral Surg Oral Med Oral Pathol; 1967 Mar; 23(3):311-9. PubMed ID: 4959813 [No Abstract] [Full Text] [Related]
28. Oculodentodigital dysplasia. Fára M; Horák I; Hrivnáková J; Kapras J; Nová M; Stloukalová M Acta Chir Plast; 1977; 19(2):110-22. PubMed ID: 74156 [No Abstract] [Full Text] [Related]
29. Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imaging. Alao MJ; Bonneau D; Holder-Espinasse M; Goizet C; Manouvrier-Hanu S; Mezel A; Petit F; Subtil D; Magdelaine C; Lacombe D Eur J Med Genet; 2010; 53(1):19-22. PubMed ID: 19808103 [TBL] [Abstract][Full Text] [Related]
31. Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype. Patton MA; Laurence KM J Med Genet; 1985 Oct; 22(5):386-9. PubMed ID: 3935793 [TBL] [Abstract][Full Text] [Related]
34. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father. Ioan DM; Dagomiz D; Fryns JP Genet Couns; 2002; 13(2):187-9. PubMed ID: 12150221 [TBL] [Abstract][Full Text] [Related]
35. Interradicular dentin dysplasia associated with amelogenesis imperfecta with taurodontism or trichodentoosseous syndrome: a diagnostic dilemma. Hegde V; Srikanth K Indian J Dent Res; 2014; 25(2):269-71. PubMed ID: 24992867 [TBL] [Abstract][Full Text] [Related]
36. A case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutation. Himi M; Fujimaki T; Yokoyama T; Fujiki K; Takizawa T; Murakami A Jpn J Ophthalmol; 2009 Sep; 53(5):541-5. PubMed ID: 19847613 [TBL] [Abstract][Full Text] [Related]
37. Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement. Harting I; Karch S; Moog U; Seitz A; Pouwels PJW; Wolf NI AJNR Am J Neuroradiol; 2019 May; 40(5):903-907. PubMed ID: 31048294 [TBL] [Abstract][Full Text] [Related]
38. Oculodentodigital dysplasia. Four new reports and a literature review. Judisch GF; Martin-Casals A; Hanson JW; Olin WH Arch Ophthalmol; 1979 May; 97(5):878-84. PubMed ID: 220941 [TBL] [Abstract][Full Text] [Related]
39. Letter to the editor: Novel GJA1 mutation in oculodentodigital dysplasia. Honkaniemi J; Kalkkila JP; Koivisto P; Kähärä V; Latvala T; Simola K Am J Med Genet A; 2005 Nov; 139(1):48-9. PubMed ID: 16222672 [No Abstract] [Full Text] [Related]
40. Dental issues in lacrimo-auriculo-dento-digital syndrome: An autosomal dominant condition with clinical and genetic variability. Hajianpour MJ; Bombei H; Lieberman SM; Revell R; Krishna R; Gregorsok R; Kao S; Milunsky JM J Am Dent Assoc; 2017 Mar; 148(3):157-163. PubMed ID: 28043400 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]