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Journal Abstract Search

261 related items for PubMed ID: 6885061

  • 1. Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.
    Tabor A, Andersen O, Lundsteen C, Niebuhr E, Sardemann H.
    Hum Genet; 1983; 64(2):196-9. PubMed ID: 6885061
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  • 2. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M, Certoma A, Du Sart D, Kalitsis P, Leversha M, Fowler K, Sheffield L, Jack I, Danks DM.
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
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  • 5. Choroideremia in interstitial deletion of the X chromosome.
    Rosenberg T, Schwartz M, Niebuhr E, Yang HM, Sardemann H, Andersen O, Lundsteen C.
    Ophthalmic Paediatr Genet; 1986 Dec; 7(3):205-10. PubMed ID: 2882458
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  • 10. XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardation.
    Matsumoto T, Taku K, Miike T, Harada N, Niikawa N.
    Clin Genet; 1991 Feb; 39(2):156-8. PubMed ID: 2015697
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  • 11. Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation.
    Silengo MC, Luzzatti L, Centerwall WR, Costello JM, Parslow M.
    Clin Genet; 1981 Mar; 19(3):174-80. PubMed ID: 7273460
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  • 13. Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations.
    Milosević J, Kalicanin P.
    J Ment Defic Res; 1975 Jun; 19(2):139-44. PubMed ID: 1195357
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  • 14. Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation.
    Steinbach P, Horstmann W, Scholz W.
    Hum Genet; 1980 Jun; 54(3):309-13. PubMed ID: 7399525
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  • 16. Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardation.
    Podruch PE, Yen FS, Dinno ND, Weisskopf B.
    J Med Genet; 1982 Oct; 19(5):377-80. PubMed ID: 7143392
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  • 18. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
    Ballabio A, Bardoni B, Carrozzo R, Andria G, Bick D, Campbell L, Hamel B, Ferguson-Smith MA, Gimelli G, Fraccaro M.
    Proc Natl Acad Sci U S A; 1989 Dec; 86(24):10001-5. PubMed ID: 2602357
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  • 19. Partial deletion of the short arm of chromosome 3.
    Merrild U, Berggreen S, Hansen L, Mikkelsen M, Henningsen K.
    Eur J Pediatr; 1981 May; 136(2):211-6. PubMed ID: 7227394
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  • 20. Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.
    Sloan-Béna F, Philippe C, LeHeup B, Wuilque F, Levy ER, Chéry M, Jonveaux P, Monaco AP.
    J Med Genet; 1998 Feb; 35(2):146-50. PubMed ID: 9507395
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