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PUBMED FOR HANDHELDS

Journal Abstract Search


132 related items for PubMed ID: 4993250

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  • 5. Two cases of so-called male Turner's syndrome.
    Hashi N, Tsuda K, Tsutsumi S, Wake R, Hirota Y.
    Bull Osaka Med Sch; 1968 Apr; 14(1):86-97. PubMed ID: 5684678
    [No Abstract] [Full Text] [Related]

  • 6. [Turner's syndrome and a probable pericentric inversion of chromosome 2(45, X, 2(p+q-))].
    Hooft C, Coetsier H, Orye E.
    Ann Genet; 1968 Sep; 11(3):181-3. PubMed ID: 5304738
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  • 9. [Cytogenetic study on Turner's syndrome].
    Chen Y.
    Zhonghua Fu Chan Ke Za Zhi; 1984 Jan; 19(1):18-22. PubMed ID: 6430656
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  • 10. [Karyological variants in Turner's syndrome].
    Zanoio L, Povia P, Amantea P.
    Minerva Ginecol; 1978 Oct; 30(10):817-20. PubMed ID: 724156
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  • 11. [XY, XO, XX mosaicism with Turner's syndrome].
    Bugnon C, Colette C.
    Bull Fed Soc Gynecol Obstet Lang Fr; 1967 Oct; 19(2):158-62. PubMed ID: 5619467
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  • 12. Turner's phenotype in the male.
    Ferrier PE, Ferrier SA.
    Pediatrics; 1967 Oct; 40(4):575-85. PubMed ID: 6051057
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  • 13. [Cytogenetic studies of Turner's syndrome].
    Boczkowski K.
    Pol Tyg Lek; 1979 Oct 22; 34(43):1653-6. PubMed ID: 514876
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  • 14. [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].
    Emerit I, German J, Crippa LP, Sureau C.
    Ann Genet; 1970 Dec 22; 13(4):245-8. PubMed ID: 5313888
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  • 15. [Turner's syndrome in the newborn infant. Case report].
    Delgado A, Echarri PM, Ubago JL, Lozano MJ, Zaldúa J.
    Pathologica; 1974 Dec 22; 66(951):55-68. PubMed ID: 4844812
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  • 16. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation.
    Bjerglund Nielsen L, Nielsen IM.
    Ann Genet; 1984 Dec 22; 27(3):173-7. PubMed ID: 6334482
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  • 17. [A case of Turner's syndrome in a newborn infant. (Importance of examination of dermatoglyphics)].
    Bolgiani Naddeo MP, Franceschini P, Gandolfo Caramello MT.
    Minerva Pediatr; 1969 Apr 14; 21(15):619-23. PubMed ID: 5402256
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  • 18. A case of 45,X/46,X,dic(X)(qter----p22::p22----qter) with Turner's phenotype in a Japanese girl.
    Takenaka M, Teramoto H, Ueda K, Fujiwara A, Ohama K, Nishi Y.
    Hiroshima J Med Sci; 1988 Jun 14; 37(2):51-5. PubMed ID: 3170251
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  • 19. [Mosaicism in Shereshevskiĭ-Turner's syndrome: clinical manifestations and dermatoglyphic characteristics].
    Egorkina DA, Gurevich LE, Tomadze AA.
    Sov Med; 1984 Jun 14; (4):43-8. PubMed ID: 6740399
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  • 20. [Dermatoglyphics of the parents of children with Turner's syndrome].
    Ciovîrnache M, Florea I, Grigorescu A, Ionescu V.
    Endocrinologie; 1979 Jun 14; 17(4):271-5. PubMed ID: 523947
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