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PUBMED FOR HANDHELDS

Journal Abstract Search


134 related items for PubMed ID: 5786708

  • 1. Cytogenetic studies in premature ovarian failure.
    Boczkowski K, Radwańska E, Weintraub L, Herman E, Teter J.
    Am J Obstet Gynecol; 1969 Jun 15; 104(4):594-5. PubMed ID: 5786708
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  • 3. Cytogenetic and clinical study on 100 cases of primary amenorrhoea.
    Kallio H.
    Acta Obstet Gynecol Scand Suppl; 1973 Jun 15; ():1-78. PubMed ID: 4518464
    [No Abstract] [Full Text] [Related]

  • 4. [Secondary amenorrhea in gonadal dysgenesis (a review of the literature)].
    Markarova OS.
    Akush Ginekol (Mosk); 1973 May 15; 49(5):41-5. PubMed ID: 4594064
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  • 6. [xXi karyotype and Turner's syndrome].
    Broustet A, Nogue F, Emperaire JC, Garcia J, Darmaillacq R.
    Bord Med; 1972 Mar 15; 5(6):679-84. PubMed ID: 4560010
    [No Abstract] [Full Text] [Related]

  • 7. Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis.
    Cohen MM, Capraro VJ, Takagi N.
    Ann Hum Genet; 1967 May 15; 30(4):313-23. PubMed ID: 5619932
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  • 12. Karyotypic aberrations in chromatin positive individuals with primary ovarian failure.
    Turner JH, Charles D, Rankin JS.
    J Obstet Gynaecol Br Commonw; 1970 Jun 15; 77(6):536-43. PubMed ID: 5420746
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  • 16. Premature ovarian failure. Report of seven cases.
    Emperaire JC, Audebert A, Greenblatt RB.
    Am J Obstet Gynecol; 1970 Oct 01; 108(3):445-9. PubMed ID: 5484603
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  • 18. Primary amenorrhea: a simplified approach to diagnosis.
    Gilson MD, Knab DR.
    Am J Obstet Gynecol; 1973 Oct 01; 117(3):400-6. PubMed ID: 4354114
    [No Abstract] [Full Text] [Related]

  • 19. Familial x/x translocation: t(x;x)(p22;q13).
    Kim HJ, Hsu LY, Hirschhorn K.
    Cytogenet Cell Genet; 1974 Oct 01; 13(5):454-64. PubMed ID: 4462981
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  • 20. [Clinical and cytogenetic findings in a rare autosomal aberrations].
    Tolksdorf M.
    Monatsschr Kinderheilkd (1902); 1970 Jun 01; 118(6):308-13. PubMed ID: 5523669
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