These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

66 related items for PubMed ID: 9532457

  • 1. [Identification of marker chromosomes and translocations in man using a computerized diagnostic database and fluorescent in situ hybridization].
    Nazarenko SA, Ostroverkhova NV, Puzyrev VP, Nazarenko LP, Filimonova MN, Koriagina OIu.
    Genetika; 1998 Jan; 34(1):114-21. PubMed ID: 9532457
    [Abstract] [Full Text] [Related]

  • 2. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.
    In Vivo; 2006 Jan; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 3. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [Abstract] [Full Text] [Related]

  • 4. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
    Singh B, Gogineni S, Goberdhan A, Sacks P, Shaha A, Shah J, Rao P.
    Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603
    [Abstract] [Full Text] [Related]

  • 5. Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p arms.
    Pierluigi M, Battaglia P, Perfumo C, Baroncini A, Bricarelli FD.
    Ann Genet; 1997 Sep; 40(2):99-103. PubMed ID: 9259956
    [Abstract] [Full Text] [Related]

  • 6. [In situ ++hybridization with painting probes in the definition of reciprocal translocations].
    Pierluigi M, Perfumo C, Arslanian A, Giannotti A, Dagna Bricarelli F.
    Pathologica; 1994 Feb; 86(1):106-9. PubMed ID: 8072796
    [Abstract] [Full Text] [Related]

  • 7. Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.
    Tosi S, Giudici G, Rambaldi A, Scherer SW, Bray-Ward P, Dirscherl L, Biondi A, Kearney L.
    Genes Chromosomes Cancer; 1999 Mar; 24(3):213-21. PubMed ID: 10451701
    [Abstract] [Full Text] [Related]

  • 8. Rapid identification of marker chromosomes by in situ hybridization under different stringency conditions.
    Vorsanova SG, Yurov YB, Soloviev IV, Demidova IA, Malet P.
    Anal Cell Pathol; 1994 Oct; 7(3):251-8. PubMed ID: 7848878
    [Abstract] [Full Text] [Related]

  • 9. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
    Brown J, Horsley SW, Jung C, Saracoglu K, Janssen B, Brough M, Daschner M, Beedgen B, Kerkhoffs G, Eils R, Harris PC, Jauch A, Kearney L.
    Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
    [Abstract] [Full Text] [Related]

  • 10. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
    Lasan Trcić R, Hitrec V, Letica L, Cuk M, Begović D.
    Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
    [Abstract] [Full Text] [Related]

  • 11. [Case reports of patients with a marker chromosome].
    Kocárek E, Novotná D, Maríková T, Cernáková I, Losan F, Balícek P, Baxová A, Havlovicová M, Goetz P.
    Cas Lek Cesk; 2004 Aug; 143(10):708-11; discussion 711-2. PubMed ID: 15584624
    [Abstract] [Full Text] [Related]

  • 12. Characterisation of supernumerary chromosomal markers: a study of 13 cases.
    Douet-Guilbert N, Marical H, Pinson L, Herry A, Le Bris MJ, Morel F, De Braekeleer M.
    Cytogenet Genome Res; 2007 Aug; 116(1-2):18-23. PubMed ID: 17268173
    [Abstract] [Full Text] [Related]

  • 13. Several chromosomes involved in translocations with chromosome 5 shown with fluorescence in situ hybridization in patients with malignant myeloid disorders.
    Bram S, Rödjer S, Swolin B.
    Cancer Genet Cytogenet; 2004 Nov; 155(1):74-8. PubMed ID: 15527906
    [Abstract] [Full Text] [Related]

  • 14. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
    Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM.
    Cytogenet Genome Res; 2009 Nov; 125(2):109-14. PubMed ID: 19729913
    [Abstract] [Full Text] [Related]

  • 15. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
    Alves C, Carvalho F, Cremades N, Sousa M, Barros A.
    Eur J Hum Genet; 2002 Aug; 10(8):467-74. PubMed ID: 12111641
    [Abstract] [Full Text] [Related]

  • 16. [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; 26(9):513-6. PubMed ID: 16468325
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
    Bacino CA, Kashork CD, Davino NA, Shaffer LG.
    Am J Med Genet; 2000 Jun 05; 92(4):250-5. PubMed ID: 10842290
    [Abstract] [Full Text] [Related]

  • 19. [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 05; 24(6):635-9. PubMed ID: 18067073
    [Abstract] [Full Text] [Related]

  • 20. Identification of marker chromosomes by in situ hybridization technique using alpha and "classical" satellite DNA probes with relative chromosomal specificity.
    Vorsanova SG, Yurov YB, Passarge I, Schmidt A, Zerova TE, Demidova IA, Buzhiyevskaya TI.
    Tsitol Genet; 1994 Dec 05; 28(3):67-70. PubMed ID: 7974787
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.