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Journal Abstract Search

331 related items for PubMed ID: 21983737

  • 1. [Combined use of molecular cytogenetic techniques to detect a small chromosomal translocation].
    Xie YJ, Chen BJ, Wu JZ, Chen Z, Lin SB, Fang Q.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct; 28(5):568-71. PubMed ID: 21983737
    [Abstract] [Full Text] [Related]

  • 2. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [Abstract] [Full Text] [Related]

  • 3. [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; 24(4):392-6. PubMed ID: 17680527
    [Abstract] [Full Text] [Related]

  • 4. Spectral karyotyping and fluorescence in situ hybridization analyses identified a novel three-way translocation involving inversion 16 in therapy-related acute myeloid leukemia M4eo.
    Ohsaka A, Otsubo K, Yokota H, Hisa T, Saito H, Kozaki T.
    Cancer Genet Cytogenet; 2008 Jul 15; 184(2):113-8. PubMed ID: 18617061
    [Abstract] [Full Text] [Related]

  • 5. [The application of fluorescence in situ hybridization in detecting chronic myeloid leukemia].
    Qiu HR, Miao KR, Wang R, Qiao C, Zhang JF, Zhang SJ, Qian SX, Xu W, Li JY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr 15; 26(2):207-10. PubMed ID: 19350518
    [Abstract] [Full Text] [Related]

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  • 7. [Molecular genetics in chronic myeloid leukemia with variant Ph translocation].
    Wu W, Li JY, Zhu Y, Qiu HR, Pan JL, Xu W, Chen LJ, Shen YF, Xue YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 15; 24(4):470-3. PubMed ID: 17680547
    [Abstract] [Full Text] [Related]

  • 8. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M, Przełozna B, Płodzien M, Bugno M, Wnuk M, Kotylak Z, Słota E.
    J Appl Genet; 2005 Aug 15; 46(4):419-21. PubMed ID: 16278518
    [Abstract] [Full Text] [Related]

  • 9. Clear cell sarcoma case report: complex karyotype including t(12;22) in primary and metastatic tumor.
    Henkle CT, Hawkins AL, McCarthy EF, Griffin CA.
    Cancer Genet Cytogenet; 2004 Feb 15; 149(1):63-7. PubMed ID: 15104285
    [Abstract] [Full Text] [Related]

  • 10. Prenatal detection of a de novo Yqh-acrocentric translocation.
    Ng LK, Kwok YK, Tang LY, Ng PP, Ghosh A, Lau ET, Tang MH.
    Clin Biochem; 2006 Mar 15; 39(3):219-23. PubMed ID: 16515778
    [Abstract] [Full Text] [Related]

  • 11. [Molecular cytogenetic analysis for a familial complex chromosomal rearrangement].
    Qian WP, Tan YQ, Tjia WM, Song D, Guan XY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun 15; 22(3):302-4. PubMed ID: 15952121
    [Abstract] [Full Text] [Related]

  • 12. Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization.
    Naus NC, van Drunen E, de Klein A, Luyten GP, Paridaens DA, Alers JC, Ksander BR, Beverloo HB, Slater RM.
    Genes Chromosomes Cancer; 2001 Mar 15; 30(3):267-73. PubMed ID: 11170284
    [Abstract] [Full Text] [Related]

  • 13. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS, Hegmann K, Smith JL, Shaffer LG.
    Am J Med Genet; 1995 May 22; 57(1):31-4. PubMed ID: 7645595
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  • 15. Molecular cytogenetic analysis of follicular lymphoma (FL) provides detailed characterization of chromosomal instability associated with the t(14;18)(q32;q21) positive and negative subsets and histologic progression.
    Nanjangud G, Rao PH, Teruya-Feldstein J, Donnelly G, Qin J, Mehra S, Jhanwar SC, Zelenetz AD, Chaganti RS.
    Cytogenet Genome Res; 2007 May 22; 118(2-4):337-44. PubMed ID: 18000388
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
    Senger G, Chudoba I, Friedrich U, Tommerup N, Claussen U, Brøndum-Nielsen K.
    Prenat Diagn; 1997 Apr 22; 17(4):369-74. PubMed ID: 9160390
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  • 18. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping.
    Veldman T, Vignon C, Schröck E, Rowley JD, Ried T.
    Nat Genet; 1997 Apr 22; 15(4):406-10. PubMed ID: 9090389
    [Abstract] [Full Text] [Related]

  • 19. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
    Karst C, Gross M, Haase D, Wedding U, Höffken K, Liehr T, Mkrtchyan H.
    Int J Oncol; 2006 Apr 22; 28(4):891-7. PubMed ID: 16525638
    [Abstract] [Full Text] [Related]

  • 20. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ, Li JY, Xiao B, Zhu Y, Liu Q, Pan JL, Qiu HR, Fan L, Zhang SJ, Lu RN, Xu W, Xue YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec 22; 24(6):635-9. PubMed ID: 18067073
    [Abstract] [Full Text] [Related]

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