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Journal Abstract Search

459 related items for PubMed ID: 4272425

  • 1. 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]

  • 2. [Cytogenetic study of 257 mentally deficient patients in psychiatric hospitals].
    Bourgeois M, Bénézech M, Tournier-Zerbid N, Constant-Boy M, Benazet-Rissou J.
    Ann Med Psychol (Paris); 1975 Nov; 2(4):756-82. PubMed ID: 135524
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  • 3. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS, Kamel AA, El-Ruby M.
    Genet Couns; 2005 Nov; 16(4):393-402. PubMed ID: 16440882
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  • 5. [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
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  • 6. [Double aneuploidy: 46,XX-45,XO-47,XX,G+. Case report].
    Grosse KP, Hopfengärtner F, Schwanitz G.
    Humangenetik; 1971 Mar; 13(4):333-7. PubMed ID: 4257570
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  • 12. G-11 staining in Turner's syndrome with mos 45,X/46,X,r(?).
    de Almeida JC, Llerena JC, Molina Gomes D, Rita Martins R, Jung M, Reis DF, Cunha AG.
    Ann Genet; 1985 Mar; 28(1):37-41. PubMed ID: 2409888
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  • 14. Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality.
    MacFaul R, Turner T, Mason MK.
    Arch Dis Child; 1981 Dec; 56(12):962-3. PubMed ID: 6460476
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  • 18. [45,X/ 46,XX/ 46,XY Mosaic with female phenotype].
    Moreau N, Rochet Y, Peyramond C, Raymond D.
    Bull Assoc Anat (Nancy); 1976 Dec; 60(171):757-67. PubMed ID: 1030251
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  • 20. A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome.
    Armendares S, Buentello L, Salamanca F, Cantu-Garza JM.
    J Med Genet; 1972 Mar; 9(1):96-100. PubMed ID: 5063516
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