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.
27. Oculodentodigital Syndrome with Syndactyly Type III in a Pakistani consanguineous family. Nishat S; Mansoor Q; Javaid A; Ismail M J Dermatol Case Rep; 2012 Jun; 6(2):43-8. PubMed ID: 22826718 [TBL] [Abstract][Full Text] [Related]
28. The oculo-dento-digital syndrome: male-to-male transmission and variable expression in a family. Ioan DM; Dumitriu L; Belengeariu V; Fryns JP Genet Couns; 1997; 8(2):87-90. PubMed ID: 9219005 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. Ocular anomalies in the alagille syndrome (arteriohepatic dysplasia). Brodsky MC; Cunniff C Ophthalmology; 1993 Dec; 100(12):1767-74. PubMed ID: 8259273 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome. Park SC; Needles CF; Dimich I; Sussman L J Pediatr; 1968 Dec; 73(6):896-902. PubMed ID: 4386913 [No Abstract] [Full Text] [Related]
34. [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]
35. Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matter. Gutmann DH; Zackai EH; McDonald-McGinn DM; Fischbeck KH; Kamholz J Am J Med Genet; 1991 Oct; 41(1):18-20. PubMed ID: 1659191 [TBL] [Abstract][Full Text] [Related]
36. Ocular features of the congenital cataracts facial dysmorphism neuropathy syndrome. Müllner-Eidenböck A; Moser E; Klebermass N; Amon M; Walter MC; Lochmüller H; Gooding R; Kalaydjieva L Ophthalmology; 2004 Jul; 111(7):1415-23. PubMed ID: 15234148 [TBL] [Abstract][Full Text] [Related]
37. Brachydactyly with absence of middle phalanges and hypoplastic nails. A new hereditary syndrome. Cuevas-Sosa A; García-Segur F J Bone Joint Surg Br; 1971 Feb; 53(1):101-5. PubMed ID: 4325377 [No Abstract] [Full Text] [Related]
38. Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome. Goodman RM; Katznelson MB; Hertz M; Katznelson A J Med Genet; 1976 Apr; 13(2):136-41. PubMed ID: 933111 [TBL] [Abstract][Full Text] [Related]
39. 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]
40. [Congenital cardiopathies and associated bone abnormalities]. Pigeon Oliveros H; Pérez Treviño C; Rodríguez García I Bol Med Hosp Infant Mex; 1979; 36(1):135-47. PubMed ID: 214095 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]