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Journal Abstract Search

130 related items for PubMed ID: 8213910

  • 21. Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
    Cotter PD, Musci TJ.
    Prenat Diagn; 2001 Mar; 21(3):171-5. PubMed ID: 11260602
    [Abstract] [Full Text] [Related]

  • 22. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S.
    Rev Invest Clin; 1996 Mar; 48(1):27-33. PubMed ID: 8815483
    [Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ, Yatsenko SA, Kang SH, Cheung SW, Dudek ME, Pursley A, Ward PA, Patel A, Lupski JR.
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [Abstract] [Full Text] [Related]

  • 24. Interphase fluorescence in situ hybridization analysis: a study using centromeric probes 7, 8, and 12.
    Zhao L, Khan Z, Hayes KJ, Glassman AB.
    Ann Clin Lab Sci; 1998 Dec; 28(1):51-6. PubMed ID: 9512785
    [Abstract] [Full Text] [Related]

  • 25. [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; 24(6):635-9. PubMed ID: 18067073
    [Abstract] [Full Text] [Related]

  • 26.
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  • 27. Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9.
    Bennour A, Sennana H, Laatiri MA, Elloumi M, Khelif A, Saad A.
    Cancer Genet Cytogenet; 2009 Oct; 194(1):30-7. PubMed ID: 19737651
    [Abstract] [Full Text] [Related]

  • 28. 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; 17(4):369-74. PubMed ID: 9160390
    [Abstract] [Full Text] [Related]

  • 29. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina-Neto JM.
    Genet Couns; 2004 Apr; 15(3):303-10. PubMed ID: 15517822
    [Abstract] [Full Text] [Related]

  • 30. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.
    Chen CP, Lin CC, Su YN, Tsai FJ, Chen JT, Chern SR, Lee CC, Town DD, Chen LF, Wu PC, Wang W.
    Taiwan J Obstet Gynecol; 2010 Jun; 49(2):188-91. PubMed ID: 20708526
    [Abstract] [Full Text] [Related]

  • 31. [Diagnosis of minor chromosome modifications by molecular cytogenetics].
    Taviaux S, Moncla A, Giraud F, Demaille J, Mattei JF, Mattei MG.
    Ann Genet; 1989 Jun; 32(4):204-10. PubMed ID: 2610486
    [Abstract] [Full Text] [Related]

  • 32. Detection of chromosome-specific aneusomy and translocation by benzene metabolites in human lymphocytes using fluorescence in situ hybridization with DNA probes for chromosomes 5, 7, 8, and 21.
    Chung HW, Kim SY.
    J Toxicol Environ Health A; 2002 Mar; 65(5-6):365-72. PubMed ID: 11936217
    [Abstract] [Full Text] [Related]

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  • 34. The importance of aneuploidy screening in reciprocal translocation carriers.
    Pujol A, Benet J, Staessen C, Van Assche E, Campillo M, Egozcue J, Navarro J.
    Reproduction; 2006 Jun; 131(6):1025-35. PubMed ID: 16735542
    [Abstract] [Full Text] [Related]

  • 35. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
    Prontera P, Buldrini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, Sensi A, Calzolari E, Donti E.
    Prenat Diagn; 2006 Jun; 26(6):571-6. PubMed ID: 16683276
    [Abstract] [Full Text] [Related]

  • 36. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
    Mechoso B, Vaglio A, Quadrelli A, Mark HF, Huang XL, Milunsky A, Quadrelli R.
    Fetal Diagn Ther; 2007 Jun; 22(4):249-53. PubMed ID: 17369689
    [Abstract] [Full Text] [Related]

  • 37. Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation.
    Migliori MV, Pettinari A, Ciaschini AM, Piermattei P, Pigliapoco F, Discepoli G.
    Prenat Diagn; 2004 Apr; 24(4):290-2. PubMed ID: 15065104
    [Abstract] [Full Text] [Related]

  • 38. [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]

  • 39. Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes.
    Pettenati MJ, Von Kap-Herr C, Jackle B, Bobby P, Mowrey P, Schwartz S, Rao PN, Rosnes J.
    Prenat Diagn; 2002 Mar; 22(3):193-7. PubMed ID: 11920892
    [Abstract] [Full Text] [Related]

  • 40. Simultaneous in situ hybridization with biotin-labeled centromeric and library DNA probes: a useful method for identifying translocations.
    Wang MR, Perissel B, Malet P.
    Anal Cell Pathol; 1995 Jan; 8(1):53-6. PubMed ID: 7734411
    [Abstract] [Full Text] [Related]

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