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Journal Abstract Search
141 related items for PubMed ID: 1785627
1. Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalus. Stratton RF, Bluestone DL. Am J Med Genet; 1991 Nov 01; 41(2):169-72. PubMed ID: 1785627 [Abstract] [Full Text] [Related]
2. Re-evaluation of new X-linked syndrome for evidence of CHARGE syndrome or association. Abruzzo MA, Erickson RP. Am J Med Genet; 1989 Nov 01; 34(3):397-400. PubMed ID: 2596527 [Abstract] [Full Text] [Related]
5. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene. Alembik Y, Stoll C, Messer J. Genet Couns; 1997 Nov 01; 8(2):133-7. PubMed ID: 9219012 [Abstract] [Full Text] [Related]
9. [Oto-palato-digital type I syndrome in five generations. Relationship to the type II form]. Le Marec B, Odent S, Bracq E, Bulard MB, Bourdinière J, Babut JM. Ann Genet; 1988 Aug 01; 31(3):155-61. PubMed ID: 3265608 [Abstract] [Full Text] [Related]
14. Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts. Tüysüz B, Zeybek C, Zorer G, Sipahi O, Ungür S. Am J Med Genet; 2002 May 01; 109(3):206-10. PubMed ID: 11977180 [Abstract] [Full Text] [Related]
17. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review. Leonardi ML, Pai GS, Wilkes B, Lebel RR. Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200 [Abstract] [Full Text] [Related]
18. Oto-palato-digital syndrome with features of type I and II in brothers. Horn D, Nitz I, Bollmann R. Genet Couns; 1995 Aug 15; 6(3):233-40. PubMed ID: 8588852 [Abstract] [Full Text] [Related]