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Journal Abstract Search


83 related items for PubMed ID: 10149418

  • 1. Molecular genetics diagnostic applications in oncology.
    Hirsch-Ginsberg C, deLeon E.
    Clin Lab Sci; 1991; 4(5):284-6. PubMed ID: 10149418
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  • 3. Physician Education: Myelodysplastic Syndrome.
    Yoshida Y.
    Oncologist; 1996; 1(4):284-287. PubMed ID: 10388004
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  • 8. Acquired chromosomal rearrangements targeting selected transcription factors: contribution of molecular cytogenetic and expression analyses to the identification of clinically and biologically relevant subgroups in hematological malignancies.
    Poppe B, De Paepe A, Speleman F.
    Verh K Acad Geneeskd Belg; 2007; 69(1):47-64. PubMed ID: 17427874
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  • 9. Spectral karyotyping combined with locus-specific FISH simultaneously defines genes and chromosomes involved in chromosomal translocations.
    Tonon G, Roschke A, Stover K, Shou Y, Kuehl WM, Kirsch IR.
    Genes Chromosomes Cancer; 2000 Apr; 27(4):418-23. PubMed ID: 10719373
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  • 11. [Molecular pathology: intersection of morphology, biochemistry and genetics].
    Bosman FT.
    Ned Tijdschr Geneeskd; 1999 Nov 06; 143(45):2269-75. PubMed ID: 10578428
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  • 12. Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol.
    Kekou K, Fryssira H, Sophocleous C, Mavrou A, Manta P, Metaxotou C.
    Mol Cell Probes; 2005 Dec 06; 19(6):422-4. PubMed ID: 16144755
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  • 15. HMG1 is not rearranged by 13q12 aberrations in lipomas.
    Kazmierczak B, Dal Cin P, Meyer-Bolte K, Van den Berghe H, Bullerdiek J.
    Genes Chromosomes Cancer; 1999 Mar 06; 24(3):290-2. PubMed ID: 10451712
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  • 16. Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique Hématologique.
    Jeandidier E, Dastugue N, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, Herens C, Michaux L, Verellen-Dumoulin C, Talmant P, Cornillet-Lefebvre P, Luquet I, Charrin C, Barin C, Collonge-Rame MA, Pérot C, Van den Akker J, Grégoire MJ, Jonveaux P, Baranger L, Eclache-Saudreau V, Pagès MP, Cabrol C, Terré C, Berger R, Groupe Français de Cytogénétique Hématologique (GFCH).
    Cancer Genet Cytogenet; 2006 Apr 01; 166(1):1-11. PubMed ID: 16616106
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  • 17. Cytogenetic and molecular aspects of Philadelphia negative chronic myeloproliferative disorders: clinical implications.
    Panani AD.
    Cancer Lett; 2007 Sep 18; 255(1):12-25. PubMed ID: 17383090
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  • 18. Detection and identification of intestinal pathogens in clinical specimens using DNA microarrays.
    Jin DZ, Wen SY, Chen SH, Lin F, Wang SQ.
    Mol Cell Probes; 2006 Dec 18; 20(6):337-47. PubMed ID: 16730943
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  • 19. 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 18; 10(8):467-74. PubMed ID: 12111641
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  • 20. An ATL cell line with an IgH pseudo-rearranged band pattern by southern blotting: a pitfall of genetic diagnosis.
    Uemura A, Sugahara K, Nagai H, Murata K, Hasegawa H, Hirakata Y, Tsukasaki K, Yamada Y, Kamihira S.
    Lab Hematol; 2005 Aug 18; 11(1):8-13. PubMed ID: 15790547
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