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Journal Abstract Search

86 related items for PubMed ID: 8072796

  • 21. Breakpoint within the nucleolus organizer region resulting in a reciprocal translocation t (4;14)(q21;p12).
    Grabowski M, Fauth C, Wirtz A, Speicher MR.
    Am J Med Genet; 2000 Jun 05; 92(4):264-8. PubMed ID: 10842293
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  • 22. 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 05; 155(1):74-8. PubMed ID: 15527906
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  • 23. [Study of a familial insertional translocation involving chromosomes 1 and 7 by using fluorescence in situ hybridization].
    Tan Y, Li X, Li L, Lu G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun 05; 18(3):183-6. PubMed ID: 11402445
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  • 24. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS, Ludkovski O, Connors JM, Gascoyne RD, Lam WL, Horsman DE.
    Genes Chromosomes Cancer; 2003 Apr 05; 36(4):375-81. PubMed ID: 12619161
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  • 26. Dose reconstruction for individuals exposed to ionizing radiation using chromosome painting.
    Lucas JN.
    Radiat Res; 1997 Nov 05; 148(5 Suppl):S33-8. PubMed ID: 9355854
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  • 28. Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.
    Alter D, Mark HF.
    Exp Mol Pathol; 2000 Oct 05; 69(2):152-8. PubMed ID: 11001863
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  • 29. 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
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  • 31. 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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  • 32. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.
    Engelen JJ, Loots WJ, Albrechts JC, Plomp AS, van der Meer SB, Vles JS, Hamers GJ, Geraedts JP.
    Am J Med Genet; 1998 Feb 03; 75(4):409-13. PubMed ID: 9482648
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  • 33. Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.
    Bienvenu T, Der-Sarkissian H, Billuart P, Tissot M, Des Portes V, Brüls T, Chabrolle JP, Chauveau P, Cherry M, Kahn A, Cohen D, Beldjord C, Chelly J, Cherif D.
    Eur J Hum Genet; 1997 Feb 03; 5(2):105-9. PubMed ID: 9195162
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  • 34. Cytogenetic elaboration of a novel reciprocal translocation in sheep.
    Iannuzzi A, Perucatti A, Genualdo V, De Lorenzi L, Di Berardino D, Parma P, Iannuzzi L.
    Cytogenet Genome Res; 2013 Feb 03; 139(2):97-101. PubMed ID: 23328281
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  • 35. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
    Blennow E, Bui TH, Wallin A, Kogner P.
    Am J Med Genet; 1996 Oct 02; 65(1):60-7. PubMed ID: 8914743
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  • 38. Analysis of reciprocal translocations by chromosome painting: applications and limitations of the technique.
    Rosenberg C, Blakemore KJ, Kearns WG, Giraldez RA, Escallon CS, Pearson PL, Stetten G.
    Am J Hum Genet; 1992 Apr 02; 50(4):700-5. PubMed ID: 1550115
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  • 39. Reciprocal Translocation Analysis with Whole Chromosome Painting for FISH.
    Haskins JS, Kato TA.
    Methods Mol Biol; 2019 Apr 02; 1984():117-122. PubMed ID: 31267427
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