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Journal Abstract Search


60 related items for PubMed ID: 7972239

  • 1. Constructing a physical map around a constitutional t(1;13)(q22;q12) breakpoint in a patient with a ganglioneuroblastoma.
    Michalski AJ, Cowell JK.
    Prog Clin Biol Res; 1994; 385():79-85. PubMed ID: 7972239
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  • 2. Isolation of chromosome-specific DNA sequences from an Alu polymerase chain reaction library to define the breakpoint in a patient with a constitutional translocation t(1;13) (q22;q12) and ganglioneuroblastoma.
    Michalski AJ, Cotter FE, Cowell JK.
    Oncogene; 1992 Aug; 7(8):1595-602. PubMed ID: 1630820
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  • 3. Assignment of four sequence-tagged sites to three subregions of 13q12 using a somatic cell hybrid mapping panel.
    Michalski AJ, Cowell JK.
    Genomics; 1993 Oct; 18(1):141-3. PubMed ID: 8276401
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  • 4. WAVE3, an actin-polymerization gene, is truncated and inactivated as a result of a constitutional t(1;13)(q21;q12) chromosome translocation in a patient with ganglioneuroblastoma.
    Sossey-Alaoui K, Su G, Malaj E, Roe B, Cowell JK.
    Oncogene; 2002 Aug 29; 21(38):5967-74. PubMed ID: 12185600
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  • 9. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
    Gorski JL, Bialecki MD, McDonald MT, Massa HF, Trask BJ, Burright EN.
    Genomics; 1996 Jul 15; 35(2):338-45. PubMed ID: 8661147
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  • 13. DNA sequence of the translocation breakpoints in undifferentiated embryonal sarcoma arising in mesenchymal hamartoma of the liver harboring the t(11;19)(q11;q13.4) translocation.
    Rajaram V, Knezevich S, Bove KE, Perry A, Pfeifer JD.
    Genes Chromosomes Cancer; 2007 May 15; 46(5):508-13. PubMed ID: 17311249
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  • 15. Integrated physical, genetic, and genic map covering 3 Mb around the human NGF gene (NGFB) at 1p13.
    Carrier A, Rosier MF, Guillemot F, Goguel AF, Pulcini F, Bernheim A, Auffray C, Devignes MD.
    Genomics; 1996 Jan 01; 31(1):80-9. PubMed ID: 8808283
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  • 16. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.
    Haas M, Aburatani H, Stanton VP, Bhatt M, Housman D, Ward DC.
    Genomics; 1993 Apr 01; 16(1):90-6. PubMed ID: 8486389
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  • 19. Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infections.
    Yue Y, Stout K, Grossmann B, Zechner U, Brinckmann A, White C, Pilz DT, Haaf T.
    J Med Genet; 2006 Feb 01; 43(2):143-7. PubMed ID: 15908570
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  • 20. A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.
    McMullan TW, Crolla JA, Gregory SG, Carter NP, Cooper RA, Howell GR, Robinson DO.
    Hum Genet; 2002 Mar 01; 110(3):244-50. PubMed ID: 11935336
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