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Journal Abstract Search

116 related items for PubMed ID: 1785634

  • 1. 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
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  • 2. The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients.
    Mendez HM, Paskulin GA, Vallandro C.
    Am J Med Genet; 1985 Oct 01; 22(2):223-8. PubMed ID: 4050854
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  • 3. Are the Mirhosseini-Holmes-Walton syndrome and the Cohen syndrome identical?
    Norio R, Raitta C.
    Am J Med Genet; 1986 Oct 01; 25(2):397-8. PubMed ID: 3096139
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  • 4. 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 Oct 01; 8(4):311-6. PubMed ID: 9457500
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  • 5. Megalocornea-mental retardation syndrome: an additional case.
    Antiñolo G, Rufo M, Borrego S, Morales C.
    Am J Med Genet; 1994 Aug 15; 52(2):196-7. PubMed ID: 7802008
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  • 7. [Cohen syndrome in 2 brothers].
    Zetler S, Römke C, Aksu F.
    Klin Padiatr; 1987 Aug 15; 199(1):55-7. PubMed ID: 3560767
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  • 9. The Cohen syndrome: does mottled retina separate a Finnish and a Jewish type?
    Kondo I, Nagataki S, Miyagi N.
    Am J Med Genet; 1990 Sep 15; 37(1):109-13. PubMed ID: 2240027
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  • 12. Myhre-GOMBO syndrome: possible lumping of two "old" new syndromes.
    Bottani A, Verloes A.
    Am J Med Genet; 1995 Dec 04; 59(4):523-4. PubMed ID: 8585577
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  • 13. [Cohen's syndrome: non-causal association with vascular rings].
    Pérez-Caballero Macarrón C, Lozano Giménez C, Quintana Castilla A, Aparicio Meix JM.
    An Esp Pediatr; 2000 Mar 04; 52(3):289-95. PubMed ID: 11003912
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  • 14. Mental retardation, microcephaly and blepharochalasis in brothers.
    Reardon W, Winter RM, Wilson J, Baraitser M.
    Clin Dysmorphol; 1994 Apr 04; 3(2):128-31. PubMed ID: 8055132
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  • 15. 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 04; 43(5):1686-93. PubMed ID: 11980891
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  • 16. The Cohen syndrome: report of a case.
    Naritomi K, Chinen Y.
    Jpn J Hum Genet; 1997 Sep 04; 42(3):457-9. PubMed ID: 12503195
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  • 17. Microcephaly, lymphedema, and chorioretinal dysplasia: a distinct syndrome?
    Feingold M, Bartoshesky L.
    Am J Med Genet; 1992 Aug 01; 43(6):1030-1. PubMed ID: 1415329
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  • 18. Identical twins with Cohen syndrome.
    North KN, Fulton AB, Whiteman DA.
    Am J Med Genet; 1995 Jul 31; 58(1):54-8. PubMed ID: 7573157
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  • 19. Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: redefining a clinical entity.
    Horn D, Krebsová A, Kunze J, Reis A.
    Am J Med Genet; 2000 Jun 05; 92(4):285-92. PubMed ID: 10842298
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