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Journal Abstract Search

130 related items for PubMed ID: 8213910

  • 1. Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.
    Sullivan BA, Leana-Cox J, Schwartz S.
    Am J Med Genet; 1993 Aug 15; 47(2):223-30. PubMed ID: 8213910
    [Abstract] [Full Text] [Related]

  • 2. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG, Spikes AS, Macha M, Dunn R.
    J Reprod Med; 1996 May 15; 41(5):367-71. PubMed ID: 8725766
    [Abstract] [Full Text] [Related]

  • 3. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A, Viaggi S, Ottaggio L, Fronza G, Schenone A, Roncella S, Abbondandolo A.
    Haematologica; 2000 Mar 15; 85(3):250-5. PubMed ID: 10702812
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  • 5. Fluorescene in situ hybridization establishes homology between human and silvered leaf monkey chromosomes, reveals reciprocal translocations between chromosomes homologous to human Y/5, 1/9, and 6/16, and delineates an X1X2Y1Y2/X1X1X2X2 sex-chromosome system.
    Bigoni F, Koehler U, Stanyon R, Ishida T, Wienberg J.
    Am J Phys Anthropol; 1997 Mar 15; 102(3):315-27. PubMed ID: 9098501
    [Abstract] [Full Text] [Related]

  • 6. [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
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  • 7. Centromeric alpha-satellite DNA break in reciprocal translocations.
    Wang JC, Hajianpour A, Habibian R.
    Cytogenet Genome Res; 2009 Aug 15; 125(4):329-33. PubMed ID: 19864896
    [Abstract] [Full Text] [Related]

  • 8. 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 Aug 15; 20(4):473-8. PubMed ID: 16900777
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  • 9. 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 15; 116(9):1298-303. PubMed ID: 14527352
    [Abstract] [Full Text] [Related]

  • 10. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K, Tanemura M, Oya N, Suzumori N, Kim KC, Ohashi H, Fukushima Y.
    Prenat Diagn; 1998 Jul 15; 18(7):725-30. PubMed ID: 9706655
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  • 11. Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report.
    Blancato JK, Eglinton G, George J, Benkendorf J, Pinckert T, Meck J.
    J Reprod Med; 1995 Jul 15; 40(7):537-9. PubMed ID: 7473445
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  • 12. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A, Röddiger S, Born HJ, Baier P, Halberstadt E.
    Z Geburtshilfe Neonatol; 1996 Jul 15; 200(5):186-90. PubMed ID: 9035828
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  • 13. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.
    Wei S, Siu VM, Decker A, Quigg MH, Roberson J, Xu J, Adeyinka A.
    Prenat Diagn; 2007 Nov 15; 27(11):1064-6. PubMed ID: 17654752
    [No Abstract] [Full Text] [Related]

  • 14. Interphase fluorescence in situ hybridization in multiple myeloma and monoclonal gammopathy of undetermined significance without and with positive plasma cell identification: analysis of 192 cases from the Region of Southern Denmark.
    Christensen JH, Abildgaard N, Plesner T, Nibe A, Nielsen O, Sørensen AG, Kerndrup GB, Leukemia/Lymphoma Study Group, Region of Southern Denmark.
    Cancer Genet Cytogenet; 2007 Apr 15; 174(2):89-99. PubMed ID: 17452249
    [Abstract] [Full Text] [Related]

  • 15. 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 Apr 15; 40(2):99-103. PubMed ID: 9259956
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  • 16. Characterization of two add(4qter) chromosomes by comparative genomic hybridization.
    Bocéno M, Rival JM, Nomballais MF, David A, Avet-Loiseau H.
    Ann Genet; 1998 Apr 15; 41(2):83-6. PubMed ID: 9706338
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  • 17. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
    Frenny VJ, Antonella Z, Luisa A, Shah AD, Sheth JJ, Rocchi M.
    Indian J Cancer; 2003 Apr 15; 40(4):135-9. PubMed ID: 14716109
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  • 19. Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization.
    Bernstein R, Bocian ME, Cain MJ, Bengtsson U, Wasmuth JJ.
    Am J Med Genet; 1993 Apr 01; 46(1):77-82. PubMed ID: 8494035
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  • 20. M-FISH applications in clinical genetics.
    Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G.
    Genet Couns; 2005 Apr 01; 16(3):257-68. PubMed ID: 16259323
    [Abstract] [Full Text] [Related]

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