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Journal Abstract Search

273 related items for PubMed ID: 6051057

  • 1. Turner's phenotype in the male.
    Ferrier PE, Ferrier SA.
    Pediatrics; 1967 Oct; 40(4):575-85. PubMed ID: 6051057
    [No Abstract] [Full Text] [Related]

  • 2. [Association of a case of Turner's syndrome with familial t(Cq-; Gp+)].
    Laurent C, Bonnet P, Farouz S, Longin B.
    Ann Genet; 1970 Mar; 13(1):61-6. PubMed ID: 5310107
    [No Abstract] [Full Text] [Related]

  • 3. [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
    [No Abstract] [Full Text] [Related]

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  • 9. [On the variants on Turner's syndrome].
    Barta L, Sellyei M, Schmidt K.
    Acta Paediatr Acad Sci Hung; 1968 Sep; 9(3):305-13. PubMed ID: 5728708
    [No Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes.
    Mikel'saar AV, Blyumina MG, Kuznetsova LI, Mikel'saar RV, Lur'e IV.
    Sov Genet; 1971 May; 7(5):675-9. PubMed ID: 4272425
    [No Abstract] [Full Text] [Related]

  • 12. Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
    Bocian M, Krmpotic E, Szego K, Rosenthal IM.
    J Med Genet; 1971 Sep; 8(3):358-63. PubMed ID: 5097143
    [No Abstract] [Full Text] [Related]

  • 13. [Attempt to determinate a correlation between sex chromatin studies, sex chromosomes and phenotype in children with gonadal dysgenesis syndrome].
    Szczepski O, Goncerzewicz M, Korbas J, Krawczyński M.
    Pol Tyg Lek; 1967 Jan 16; 22(3):81-3. PubMed ID: 6031856
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  • 15. A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.
    WIELIE G, COENEGRACHT JM, STALDER G.
    Cytogenetics; 1964 Jan 16; 3():427-40. PubMed ID: 14267135
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  • 17. Severe mental retardation in Turner's syndrome and an additional mosaic with a centric chromosome fragment.
    Fischer M, Haslund J.
    Acta Genet Stat Med; 1968 Jan 16; 18(5):487-95. PubMed ID: 5756060
    [No Abstract] [Full Text] [Related]

  • 18. [Turner's syndrome with XY karyotype].
    de Grouchy J, Job JC.
    Ann Genet; 1965 Jan 16; 8(2):95-7. PubMed ID: 5295211
    [No Abstract] [Full Text] [Related]

  • 19. A family with a presumptive C-F translocation in five generations.
    Therkelsen AJ, Klinge T, Henningsen K, Mikkelsen M, Schmidt G.
    Ann Genet; 1971 Mar 16; 14(1):13-21. PubMed ID: 5314290
    [No Abstract] [Full Text] [Related]

  • 20. [Identification of Turner's syndrome in the newborn infant].
    Gonzalez CH, Corradini HB, Saladanha PH.
    Rev Hosp Clin Fac Med Sao Paulo; 1972 Mar 16; 27(4):177-80. PubMed ID: 5056448
    [No Abstract] [Full Text] [Related]

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