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.


PUBMED FOR HANDHELDS

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]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. The Cohen syndrome: report of a case.
    Naritomi K, Chinen Y.
    Jpn J Hum Genet; 1997 Sep; 42(3):457-9. PubMed ID: 12503195
    [Abstract] [Full Text] [Related]

  • 5. [Cohen's syndrome in 2 sisters].
    Doyard P, Mattei JF.
    Sem Hop; 1984 Apr 12; 60(16):1143-7. PubMed ID: 6326307
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No 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]

  • 9.
    ; . PubMed ID:
    [No 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]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. The Cohen syndrome in Israel.
    Sack J, Friedman E.
    Isr J Med Sci; 1986 Nov 01; 22(11):766-70. PubMed ID: 2432032
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No 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]
    of 14.