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Journal Abstract Search

84 related items for PubMed ID: 2106420

  • 1. Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots.
    Carter NP, Ferguson-Smith ME, Affara NA, Briggs H, Ferguson-Smith MA.
    Cytometry; 1990; 11(1):202-7. PubMed ID: 2106420
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  • 2. Quantification of the DNA content of structurally abnormal X chromosomes and X chromosome aneuploidy using high resolution bivariate flow karyotyping.
    Trask B, van den Engh G, Nussbaum R, Schwartz C, Gray J.
    Cytometry; 1990; 11(1):184-95. PubMed ID: 2106419
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  • 3. Flow cytometric quantification of human chromosome specific repetitive DNA sequences by single and bicolor fluorescent in situ hybridization to lymphocyte interphase nuclei.
    van Dekken H, Arkesteijn GJ, Visser JW, Bauman JG.
    Cytometry; 1990; 11(1):153-64. PubMed ID: 2307056
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  • 10. Accurate characterization of porcine bivariate flow karyotype by PCR and fluorescence in situ hybridization.
    Yerle M, Schmitz A, Milan D, Chaput B, Monteagudo L, Vaiman M, Frelat G, Gellin J.
    Genomics; 1993 Apr; 16(1):97-103. PubMed ID: 8486390
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  • 11. Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.
    Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M.
    C R Acad Sci III; 1993 Apr; 316(4):375-83. PubMed ID: 8402263
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  • 12. Two mosaic cases with nonfluorescent Y chromosome analysed with Y-specific DNA probes.
    Kałuzewski B, Jakubowski L, Debiec-Rychter M, Grzeschik KH, Limon J, Gibas Z.
    Am J Med Genet; 1988 Nov; 31(3):489-503. PubMed ID: 3228133
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  • 13. Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies.
    Shankman S, Spurdle AB, Morris D, Rosendorff J, Marques I, Bernstein R, Ramsay M.
    Am J Med Genet; 1995 Jan 30; 55(3):269-75. PubMed ID: 7726221
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  • 14. Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness.
    Weil D, Wang I, Dietrich A, Poustka A, Weissenbach J, Petit C.
    Nat Genet; 1994 Jul 30; 7(3):414-9. PubMed ID: 7920661
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  • 15. XX sex reversal: molecular analysis of the SRY/ZFY regions.
    Reddy PP, Papenhausen PR, Suh YM, Riddick LM, Calvano CJ, Mandell J.
    J Urol; 1997 Sep 30; 158(3 Pt 2):1305-7. PubMed ID: 9258201
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  • 19. [Female karyotype and male phenotype: XX men. Apropos of 2 cases].
    Teyssier M, Moreau N.
    J Gynecol Obstet Biol Reprod (Paris); 1986 Sep 30; 15(6):751-6. PubMed ID: 3098823
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