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Journal Abstract Search

123 related items for PubMed ID: 16845657

  • 1. High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).
    Wieland I, Muschke P, Volleth M, Röpke A, Pelz AF, Stumm M, Wieacker P.
    Genes Chromosomes Cancer; 2006 Oct; 45(10):945-9. PubMed ID: 16845657
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  • 3. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.
    Lindblom A, Sandelin K, Iselius L, Dumanski J, White I, Nordenskjöld M, Larsson C.
    Am J Hum Genet; 1994 May; 54(5):871-6. PubMed ID: 8178827
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  • 4. Molecular cloning of a constitutional t(7;22) translocation associated with risk of hematological malignancy.
    Hill AS, MacCallum PK, Young BD, Lillington DM.
    Genes Chromosomes Cancer; 2003 Nov; 38(3):260-4. PubMed ID: 14506701
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  • 5. A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.
    Jobanputra V, Chung WK, Hacker AM, Emanuel BS, Warburton D.
    Prenat Diagn; 2005 Aug; 25(8):683-6. PubMed ID: 16049998
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  • 6. Balanced t(11;15)(q23;q15) in a TP53+/+ breast cancer patient from a Li-Fraumeni syndrome family.
    Sherif ZA, Danielsen M.
    Cancer Genet Cytogenet; 2006 Jul 01; 168(1):50-8. PubMed ID: 16772121
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  • 9. Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study.
    Schoemaker MJ, Jones ME, Higgins CD, Wright AF, UK Clinical Cytogenetics Group, Swerdlow AJ.
    Int J Cancer; 2019 Sep 15; 145(6):1493-1498. PubMed ID: 30496607
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  • 11. Cryptic deletion of EGR1 in association with a novel balanced t(5;22)(q31;q11.2) in a patient with myelodysplastic syndrome.
    Hoffman MW, Janney S, Batanian JR.
    Cancer Genet Cytogenet; 2009 Jun 15; 191(2):106-8. PubMed ID: 19446747
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  • 12. Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene.
    Bonne A, Vreede L, Kuiper RP, Bodmer D, Jansen C, Eleveld M, van Erp F, Arkesteijn G, Hoogerbrugge N, van Ravenswaaij C, Schoenmakers EF, Geurts van Kessel A.
    Cancer Genet Cytogenet; 2007 Nov 15; 179(1):11-8. PubMed ID: 17981209
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  • 13. The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombination.
    Hill AS, Foot NJ, Chaplin TL, Young BD.
    Hum Mol Genet; 2000 Jun 12; 9(10):1525-32. PubMed ID: 10888603
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  • 15. Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22).
    Balci S, Engiz O, Yilmaz Z, Baltaci V.
    Genet Couns; 2006 Jun 12; 17(3):281-9. PubMed ID: 17100195
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  • 18. Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2).
    Takeuchi M, Katayama Y, Okamura A, Yamamoto K, Shimoyama M, Matsui T.
    Cancer Genet Cytogenet; 2007 Nov 12; 179(1):85-7. PubMed ID: 17981222
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  • 20. Increased radiosensitivity as an indicator of genes conferring breast cancer susceptibility.
    Varga D, Vogel W, Bender A, Surowy H, Maier C, Kreienberg R, Deissler H, Sauer G.
    Strahlenther Onkol; 2007 Dec 12; 183(12):655-60. PubMed ID: 18040608
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