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Journal Abstract Search

150 related items for PubMed ID: 4134628

  • 1.
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  • 2. A new variant of Klinefelter's syndrome with a presumptive deleted Y chromosome.
    Miller RC, Goodman RM, Miller FR, Nusbaum L.
    Ann Intern Med; 1967 Oct; 67(4):825-31. PubMed ID: 6052857
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  • 4. An 18p21q translocation in a patient with presumptive "monosomy G".
    Cohen MM, Putnam TI.
    Am J Dis Child; 1972 Dec; 124(6):908-10. PubMed ID: 4639227
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  • 6. Banding identification of partial trisomy 15 and of 8/21 translocation.
    Wurster-Hill DH, Hoefnagel D.
    J Ment Defic Res; 1974 Jun; 18(2):139-44. PubMed ID: 4141377
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  • 7. Inherited partial duplication of chromosome No. 15.
    Fujimoto A, Towner JW, Ebbin AJ, Kahlstrom EJ, Wilson MG.
    J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
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  • 8. [Anomalies in dermatoglyphics in Turner's syndrome and Klinefelter's syndrome (study based on 25 cases of personal observation)].
    Faggiano M, Minozzi M, Salerno M, Lombardi G, Nunziata V.
    Folia Endocrinol; 1972 Feb; 25(1):69-82. PubMed ID: 5067412
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  • 11. G-deletion syndrome II.
    Chauvel PJ, Schindeler JD, Warren RJ.
    Humangenetik; 1972 Feb; 14(2):164-6. PubMed ID: 5026850
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  • 12. A Gq deletion in a girl with Down's syndrome.
    Hongell K, Airaksinen E.
    Hum Hered; 1972 Feb; 22(1):80-5. PubMed ID: 4260912
    [No Abstract] [Full Text] [Related]

  • 13. An inherited 1;G translocation.
    Ebbin AJ, Wilson MG, Towner JW, Forsman I.
    J Med Genet; 1971 Dec; 8(4):536-9. PubMed ID: 5149540
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  • 15. [Klinefelter's syndrome. Karyotype XXYY. Study of dermatoglyphics].
    Muller JM, Jalbert P, Cordonnier D.
    Ann Biol Clin (Paris); 1967 Dec; 25(1):207-14. PubMed ID: 6031413
    [No Abstract] [Full Text] [Related]

  • 16. Klinefelter's syndrome and G trisomy.
    Erdtmann B, de Freitas AA, de Souza RP, Salzano FM.
    J Med Genet; 1971 Sep; 8(3):364-8. PubMed ID: 5097144
    [No Abstract] [Full Text] [Related]

  • 17. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
    Wyandt HE, Hecht F, Lovrien EW, Stewart RE.
    Cytogenetics; 1971 Sep; 10(6):413-26. PubMed ID: 5146418
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  • 18. Cytogenetic studies in mental retardation with report of a case of XXXXY variant of Klinefelter's syndrome.
    Walter A, Mammen KC, Martin B, Gopalakrishnamoorthy HR, John TJ.
    Indian J Med Res; 1971 Jul; 59(7):1072-6. PubMed ID: 4266624
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  • 19. Sole dermatoglyphics of patients with Klinefelter's syndrome (47,XXY).
    Komatz Y, Kiriyama T, Yoshida O.
    J Ment Defic Res; 1979 Jun; 23(2):85-90. PubMed ID: 490634
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