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Journal Abstract Search
269 related items for PubMed ID: 9457500
1. A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome. Mejía-Baltodano G, Bobadilla L, Solís A, Mendoza R, Díaz-Gallardo MY, Barros-Núñez P. Genet Couns; 1997; 8(4):311-6. PubMed ID: 9457500 [Abstract] [Full Text] [Related]
2. The Cohen syndrome: report of five new cases and a review of the literature. Friedman E, Sack J. J Craniofac Genet Dev Biol; 1982; 2(3):193-200. PubMed ID: 7166592 [Abstract] [Full Text] [Related]
8. [Cohen syndrome. A new case and review of the literature]. Calzolari S, Ballardini M, De Marco P. Minerva Pediatr; 1995 Mar 12; 47(3):83-7. PubMed ID: 7791717 [Abstract] [Full Text] [Related]
10. Tapetoretinal degeneration in brothers with apparent Cohen syndrome: nosology with Mirhosseini-Holmes-Walton syndrome. Steinlein O, Tariverdian G, Boll HU, Vogel F. Am J Med Genet; 1991 Nov 01; 41(2):196-200. PubMed ID: 1785634 [Abstract] [Full Text] [Related]
11. Mechanisms of myopia in Cohen syndrome mapped to chromosome 8q22. Summanen P, Kivitie-Kallio S, Norio R, Raitta C, Kivelä T. Invest Ophthalmol Vis Sci; 2002 May 01; 43(5):1686-93. PubMed ID: 11980891 [Abstract] [Full Text] [Related]
18. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed. Zwamborn-Hanssen AM, Schrander-Stumpel CT, Smeets E, Decock P, Fryns JP. Genet Couns; 1995 Nov 01; 6(4):313-9. PubMed ID: 8775418 [Abstract] [Full Text] [Related]
19. Fountain syndrome: further delineation of the clinical syndrome and follow-up data. Van Buggenhout GJ, Van Ravenswaaij-Arts CM, Renier WO, Van de Wiel MP, Trommelen JC, Pijkels E, Hamel BC, Fryns JP. Genet Couns; 1996 Nov 01; 7(3):177-86. PubMed ID: 8897038 [Abstract] [Full Text] [Related]
20. Café au lait macules and cerebro-oculo-facio-skeletal syndrome: a novel association. Twede JV, Difazio M. Pediatr Dermatol; 2009 Nov 01; 26(1):97-9. PubMed ID: 19250421 [Abstract] [Full Text] [Related] Page: [Next] [New Search]