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Journal Abstract Search

90 related items for PubMed ID: 9042195

  • 21.
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  • 22. [Genetic anomalies in dysmenorrhea and sterility: range and frequency, age-related dependence, mosaicism dynamics].
    Sazonova LA, Suskov II.
    Genetika; 1983; 19(1):171-3. PubMed ID: 6682067
    [Abstract] [Full Text] [Related]

  • 23. Molecular cytogenetic analysis of a nontumorigenic human breast epithelial cell line that eventually turns tumorigenic: validation of an analytical approach combining karyotyping, comparative genomic hybridization, chromosome painting, and single-locus fluorescence in situ hybridization.
    Nielsen KV, Niebuhr E, Ejlertsen B, Holstebroe S, Madsen MW, Briand P, Mouridsen HT, Bolund L.
    Genes Chromosomes Cancer; 1997 Sep; 20(1):30-7. PubMed ID: 9290951
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  • 24. Chromosome aberrations in a series of 120 multiple myeloma cases with abnormal karyotypes.
    Mohamed AN, Bentley G, Bonnett ML, Zonder J, Al-Katib A.
    Am J Hematol; 2007 Dec; 82(12):1080-7. PubMed ID: 17654686
    [Abstract] [Full Text] [Related]

  • 25. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
    Reshmi SC, Miller JL, Deplewski D, Close C, Henderson LJ, Littlejohn E, Schwartz S, Waggoner DJ.
    Eur J Med Genet; 2011 Dec; 54(2):161-4. PubMed ID: 21078420
    [Abstract] [Full Text] [Related]

  • 26. Molecular cytogenetic characterization of the human cerebral microvessel endothelial cell line hCMEC/D3.
    Mkrtchyan H, Scheler S, Klein I, Fahr A, Couraud PO, Romero IA, Weksler B, Liehr T.
    Cytogenet Genome Res; 2009 Dec; 126(4):313-7. PubMed ID: 19864871
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  • 27.
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  • 28. Karyotypes of human T-lymphocyte clones.
    Lambert B, Holmberg K, He SH, Einhorn N.
    IARC Sci Publ; 1988 Dec; (89):469-76. PubMed ID: 3264269
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  • 29.
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  • 30. [The patterns of the karyotypic evolution of cells in culture].
    Mamaeva SE.
    Tsitologiia; 1996 Dec; 38(8):787-814. PubMed ID: 9027012
    [Abstract] [Full Text] [Related]

  • 31. Detection of human chromosomal abnormalities using a new technique combining 4',6-diamidino-2-phenyl-indole staining and image analysis.
    Liu JY, Ji MF, Wang XR, Luo RL, Ren X, Liu M, Wang QK.
    Clin Genet; 2006 Jan; 69(1):65-71. PubMed ID: 16451138
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  • 32.
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  • 33. Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46, XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome.
    Kotzot D, Schinzel A.
    Eur J Hum Genet; 2000 Sep; 8(9):709-12. PubMed ID: 10980577
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