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Journal Abstract Search

150 related items for PubMed ID: 14104167

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  • 4. A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.
    WIELIE G, COENEGRACHT JM, STALDER G.
    Cytogenetics; 1964; 3():427-40. PubMed ID: 14267135
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  • 5. CRANIOTELENCEPHALIC DYSPLASIA. AN UNUSUAL EXAMPLE OF DYSPLASIA OF FRONTAL BONE.
    JABBOUR JT, TAYBI H.
    Am J Dis Child; 1964 Dec; 108():627-32. PubMed ID: 14213965
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  • 6. Autoradiographic re-appraisal of an XXXxY male as a probable XXXXY with a 4-11 translocation.
    Ockey CH, De la Chapelle A.
    Cytogenetics; 1967 Dec; 6(3):178-92. PubMed ID: 6040472
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  • 12. A BOY WITH XXXXY SEX CHROMOSOMES.
    JOSEPH MC, ANDERS JM, TAYLOR AI.
    J Med Genet; 1964 Dec; 1(2):95-101. PubMed ID: 14234112
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  • 13. The 13q-deletion syndrome.
    Allderdice PW, Davis JG, Miller OJ, Klinger HP, Warburton D, Miller DA, Allen FH, Abrams CA, McGilvray E.
    Am J Hum Genet; 1969 Sep; 21(5):499-512. PubMed ID: 5347076
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  • 14. LE CRI DU CHAT (CRYING CAT) SYNDROME.
    DUMARS KW, GASKILL C, KITZMILLER N.
    Am J Dis Child; 1964 Nov; 108():533-7. PubMed ID: 14209689
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  • 16. Familial transmission of a translocation between two non-homologous large acrocentric chromosomes. Clinical, cytogenetic and autoradiographic studies.
    Jacobsen P, Mikkelsen M, Froland A, Dupont A.
    Ann Hum Genet; 1966 May; 29(4):391-402. PubMed ID: 5961828
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  • 18. XX SEX CHROMOSOMES IN A HUMAN MALE. FIRST CASE.
    DELACHAPELLE A, HORTLING H, NIEMI M, WENNSTROEM J.
    Acta Med Scand; 1964 May; 175():SUPPL 412:25-8. PubMed ID: 14154995
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