These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
128 related articles for article (PubMed ID: 23071171)
21. Fraser syndrome. Cryptophthalmos syndactyly syndrome. Tilahun M; Kifle A; Oljira B Ethiop Med J; 1990 Apr; 28(2):89-90. PubMed ID: 2163830 [No Abstract] [Full Text] [Related]
22. [Genetic study of a pedigree affected with oculodentodigital dysplasia]. Gu L; Zhu Y; Zhu X; Li J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1191-1194. PubMed ID: 31813145 [TBL] [Abstract][Full Text] [Related]
23. Oculodentodigital dysplasia: study of ophthalmological and clinical manifestations in three boys with probably autosomal recessive inheritance. Frasson M; Calixto N; Cronemberger S; de Aguiar RA; Leão LL; de Aguiar MJ Ophthalmic Genet; 2004 Sep; 25(3):227-36. PubMed ID: 15512999 [TBL] [Abstract][Full Text] [Related]
24. Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia? Spaepen A; Schrander-Stumpel C; Fryns JP; de Die-Smulders C; Borghgraef M; Van den Berghe H Am J Med Genet; 1991 Dec; 41(4):517-20. PubMed ID: 1663704 [TBL] [Abstract][Full Text] [Related]
27. [Neurological presentations of oculodentodigital dysplasia]. Rudenskaya GE; Dyomina NA; Bliznetz EA; Khlebnikova OV; Dadaly EL; Polyakov AV Zh Nevrol Psikhiatr Im S S Korsakova; 2018; 118(5):85-91. PubMed ID: 29927410 [TBL] [Abstract][Full Text] [Related]
28. Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly. Richardson R; Donnai D; Meire F; Dixon MJ J Med Genet; 2004 Jan; 41(1):60-7. PubMed ID: 14729836 [No Abstract] [Full Text] [Related]
29. Effects of Reduced Connexin43 Function on Mandibular Morphology and Osteogenesis in Mutant Mouse Models of Oculodentodigital Dysplasia. Moore AC; Wu J; Jewlal E; Barr K; Laird DW; Willmore KE Calcif Tissue Int; 2020 Dec; 107(6):611-624. PubMed ID: 32902679 [TBL] [Abstract][Full Text] [Related]
30. The different appearance of the oculodentodigital dysplasia syndrome. Thomsen M; Schneider U; Weber M; Niethard FU J Pediatr Orthop B; 1998 Jan; 7(1):23-6. PubMed ID: 9481652 [TBL] [Abstract][Full Text] [Related]
31. Mutations in RARS cause hypomyelination. Wolf NI; Salomons GS; Rodenburg RJ; Pouwels PJ; Schieving JH; Derks TG; Fock JM; Rump P; van Beek DM; van der Knaap MS; Waisfisz Q Ann Neurol; 2014 Jul; 76(1):134-9. PubMed ID: 24777941 [TBL] [Abstract][Full Text] [Related]
32. Intraoral findings of oculodentodigital dysplasia. Weintraub DM; White GE; Dines MM; Tanaka H ASDC J Dent Child; 1976; 43(6):427-9. PubMed ID: 824333 [No Abstract] [Full Text] [Related]
33. Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24. Gladwin A; Donnai D; Metcalfe K; Schrander-Stumpel C; Brueton L; Verloes A; Aylsworth A; Toriello H; Winter R; Dixon M Hum Mol Genet; 1997 Jan; 6(1):123-7. PubMed ID: 9002680 [TBL] [Abstract][Full Text] [Related]
34. [A de novo GJA1 mutation identified by whole-exome sequencing in a patient with oculodentodigital dysplasia]. Zeng H; Xie L; Tang M; Yang Y; Tan Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):268-271. PubMed ID: 29653008 [TBL] [Abstract][Full Text] [Related]
35. Double teeth and syndactyly. Bradbury AJ Dent Update; 1983; 10(1):53-5. PubMed ID: 6301903 [No Abstract] [Full Text] [Related]
36. Oculo-dento-digital Dysplasia Presenting as Spastic Paraparesis Which Was Successfully Treated by Intrathecal Baclofen Therapy. Shinya A; Takahashi M; Sato N; Nishida Y; Inaba A; Inaji M; Yokota T; Orimo S Intern Med; 2021 Jul; 60(14):2301-2305. PubMed ID: 33612672 [TBL] [Abstract][Full Text] [Related]
38. Evidence for genetic anticipation in the oculodentodigital syndrome. Shapiro RE; Griffin JW; Stine OC Am J Med Genet; 1997 Jul; 71(1):36-41. PubMed ID: 9215766 [TBL] [Abstract][Full Text] [Related]
39. A rare symptom of a very rare disease: a case report of a oculodentodigital dysplasia with lymphedema. Gumus E Clin Dysmorphol; 2018 Jul; 27(3):91-93. PubMed ID: 29624507 [No Abstract] [Full Text] [Related]