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Journal Abstract Search

231 related items for PubMed ID: 16451138

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  • 7. A cytogenetic study of five rare karyotypes.
    Yang ZR, Xiao YZ, Liu XX.
    J Tongji Med Univ; 1992; 12(4):234-6. PubMed ID: 1289572
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  • 9. [Simultaneous presence of ins (15;17),t(2;17;20) and trisomy 8 in a patient with acute promyelocytic leukemia].
    Bai S, Xue Y, Wu Y, Pan J, Zhang J, Shen J, Wang Y, Qiu H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):712-4. PubMed ID: 19065540
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  • 10. Specific chromosomal aberrations in de novo acute myeloid leukemia: a comparative analysis of results with a report of three novel chromosomal rearrangements t(7;14)(q35;q13), t(8;18)(p11.2;q12), t(13;15) in Indian population.
    Ahmad F, Dalvi R, Das BR, Mandava S.
    Cancer Detect Prev; 2008 Dec; 32(2):168-77. PubMed ID: 18639991
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  • 11. [Rearrangements of the mixed lineage leukemia gene in acute myeloid leukemia].
    Zhang LJ, Lu XL, He J, Li Y.
    Zhonghua Yi Xue Za Zhi; 2006 Aug 29; 86(32):2256-60. PubMed ID: 17064570
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  • 12. [Multiplex fluorescence in situ hybridization in detecting complex chromosomal aberrations in myelodysplastic syndromes].
    Xiao B, Li JY, Pan JL, Ma L, Qiu HR, Wu YF, Xue YQ.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Sep 29; 26(9):513-6. PubMed ID: 16468325
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  • 13. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ, Di YF, Song YZ, Cheng DH, Li LY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 29; 24(4):392-6. PubMed ID: 17680527
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  • 17. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
    Zhao L, Li H, Xue YQ, Pan JL, Wu YF, Lu M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec 29; 21(6):611-4. PubMed ID: 15583994
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  • 18. Derivative (3)t(3;18)(q27;q21)t(18;16)(q21;?) involving the BCL2 and BCL6 genes in follicular lymphoma with t(3;14;18)(q27;q32;q21).
    Yamamoto K, Ono K, Katayama Y, Shimoyama M, Matsui T.
    Cancer Genet Cytogenet; 2007 Nov 29; 179(1):69-75. PubMed ID: 17981218
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  • 19. Is cytogenetic diagnosis of 46,XX karyotype spontaneous abortion specimens erroneous? Fluorescence in situ hybridization as a confirmatory technique.
    Karaoguz MY, Nas T, Konaç E, Ince D, Pala E, Menevse S.
    J Obstet Gynaecol Res; 2005 Dec 29; 31(6):508-13. PubMed ID: 16343250
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  • 20. [Clinical and laboratory characteristics of two acute lymphoblastic leukemia patients with dicentric (9; 20) (p11 - 13; q11)].
    Gong SL, Qiu HY, Li JY, Han FL, Song XM, Huang ZX, Wang JM.
    Zhonghua Xue Ye Xue Za Zhi; 2006 May 29; 27(5):306-9. PubMed ID: 16875578
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