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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

256 related items for PubMed ID: 566736

  • 21. Fragile sites and X-linked retardation.
    Hecht F, Hecht BK, Glover TW.
    Hosp Pract (Off Ed); 1981 Nov; 16(11):81-4, 86-8. PubMed ID: 6797930
    [No Abstract] [Full Text] [Related]

  • 22. The Noonan syndrome--a review of the clinical and genetic features of 27 cases.
    Collins E, Turner G.
    J Pediatr; 1973 Dec; 83(6):941-50. PubMed ID: 4148394
    [No Abstract] [Full Text] [Related]

  • 23. Retinitis pigmentosa with mental retardation, deafness and XX-XO sex chromosomes.
    Jancar J.
    J Ment Defic Res; 1970 Dec; 14(4):269-73. PubMed ID: 5517966
    [No Abstract] [Full Text] [Related]

  • 24. Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
    Sarda P, Lefort G, Devaux P, Humeau C, Rieu D.
    Ann Genet; 1992 Dec; 35(2):117-20. PubMed ID: 1524409
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  • 25. [Turners syndrome in men].
    Zarubina NA, Glikman EV, Iur'eva NP.
    Probl Endokrinol (Mosk); 1974 Dec; 20(4):29-34. PubMed ID: 4449796
    [No Abstract] [Full Text] [Related]

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  • 33. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.
    Mattei JF, Collignon P, Ayme S, Giraud F.
    Clin Genet; 1983 Jan; 23(1):70-4. PubMed ID: 6682021
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  • 34. A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24.
    Mitchell SJ, McHale DP, Campbell DA, Lench NJ, Mueller RF, Bundey SE, Markham AF.
    Am J Hum Genet; 1998 May; 62(5):1070-6. PubMed ID: 9545391
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  • 35. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
    Lambotte C, Carlier G, Frederic J, Keutgen J.
    Acta Paediatr Belg; 1971 May; 25(2):119-26. PubMed ID: 5565831
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  • 40. [X-linked retinitis pigmentosa].
    Ignaczak R, Sobolewski P.
    Klin Oczna; 1992 May; 94(2-3):78-9. PubMed ID: 1640690
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