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Journal Abstract Search

105 related items for PubMed ID: 1405391

  • 21. [Clinical and cytogenetic problems in diagnosis of fragile X syndrome].
    von Gontard A, Hillig U, Herold D.
    Z Kinder Jugendpsychiatr; 1992 Jun; 20(2):113-20. PubMed ID: 1509819
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  • 22. [Fragile X-syndrome and mental retardation].
    Eskeland P.
    Tidsskr Nor Laegeforen; 1992 Mar 20; 112(8):1007-8. PubMed ID: 1553720
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  • 23. Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population.
    Pouya AR, Abedini SS, Mansoorian N, Behjati F, Nikzat N, Mohseni M, Nieh SE, Abbasi Moheb L, Darvish H, Monajemi GB, Banihashemi S, Kahrizi K, Ropers HH, Najmabadi H.
    Eur J Med Genet; 2009 Mar 20; 52(4):170-3. PubMed ID: 19361583
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  • 24. Aberrant behaviors of young boys with fragile X syndrome.
    Lachiewicz AM, Spiridigliozzi GA, Gullion CM, Ransford SN, Rao K.
    Am J Ment Retard; 1994 Mar 20; 98(5):567-79. PubMed ID: 8192902
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  • 25. Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient.
    Mavrou A, Syrrou M, Tsenghi C, Agelakis M, Youroukos S, Metaxotou C.
    Am J Med Genet; 1988 Dec 20; 31(4):735-9. PubMed ID: 3239562
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  • 31. Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology.
    Patsalis PC, Sismani C, Hadjimarcou MI, Rose N, Stylianidou G, Koukoulli R, Anastasiadou V, Deltas CC, Middleton L.
    Genet Couns; 1997 Dec 20; 8(1):1-6. PubMed ID: 9101271
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  • 32. [The fragile X (Martin-Bell) syndrome].
    Zergollern-Cupak L, Sabol Z, Hitrec V, Vuković J, Medica I.
    Lijec Vjesn; 1990 Dec 20; 112(11-12):393-6. PubMed ID: 2097475
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  • 37. Cytogenetic findings in moderate and severe mental retardation. A study of an institutionalized population of 1991 patients.
    Fryns JP, Kleczkowska A, Kubień E, Van den Berghe H.
    Acta Paediatr Scand Suppl; 1984 Dec 20; 313():1-23. PubMed ID: 6241420
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  • 39. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families).
    Rocchi M, Archidiacono N, Filippi G.
    J Genet Hum; 1987 Dec 20; 35(5):351-79. PubMed ID: 3437265
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