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PUBMED FOR HANDHELDS

Journal Abstract Search


235 related items for PubMed ID: 8481611

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  • 4. A genetic-diagnostic survey in an institutionalized population of 158 mentally retarded patients. The Viaene experience.
    Dereymaeker AM, Fryns JP, Haegeman J, Deroover J, Van den Berghe H.
    Clin Genet; 1988 Aug; 34(2):126-34. PubMed ID: 2973379
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  • 11. Fragile X syndrome. Clinical and cytogenetic studies.
    Félix TM, de Pina-Neto JM.
    Arq Neuropsiquiatr; 1998 Mar; 56(1):9-17. PubMed ID: 9686114
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  • 12. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.
    Rauch A, Hoyer J, Guth S, Zweier C, Kraus C, Becker C, Zenker M, Hüffmeier U, Thiel C, Rüschendorf F, Nürnberg P, Reis A, Trautmann U.
    Am J Med Genet A; 2006 Oct 01; 140(19):2063-74. PubMed ID: 16917849
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  • 15. Comparison between the cytogenetic test for fragile X and the molecular analysis of the FMR-1 gene in Japanese mentally retarded individuals.
    Hofstee Y, Arinami T, Hamaguchi H.
    Am J Med Genet; 1994 Jul 15; 51(4):466-70. PubMed ID: 7943021
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  • 19. Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome.
    Butler MG, Pratesi R, Watson MS, Breg WR, Singh DN.
    Clin Genet; 1993 Sep 15; 44(3):129-38. PubMed ID: 8275570
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