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Journal Abstract Search

153 related items for PubMed ID: 17981209

  • 21.
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  • 22. Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation.
    Bernheim A, Toujani S, Guillaud-Bataille M, Richon C, Waxin H, Dessen P, Berger R.
    Cytogenet Genome Res; 2007; 119(3-4):185-90. PubMed ID: 18253027
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  • 23. Breakpoint mapping by FISH in a Sotos patient with a constitutional translocation t(3;6).
    Kok K, Mosselaar A, Faber H, Dijkhuizen T, Draaijers TG, van der Veen AY, Buys CH, Schrander-Stumpel CT.
    J Med Genet; 1999 Apr; 36(4):346-7. PubMed ID: 10227409
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  • 26. A familial case of renal cell carcinoma and a t(2;3) chromosome translocation.
    Koolen MI, van der Meyden AP, Bodmer D, Eleveld M, van der Looij E, Brunner H, Smits A, van den Berg E, Smeets D, Geurts van Kessel A.
    Kidney Int; 1998 Feb; 53(2):273-5. PubMed ID: 9461085
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  • 27. Characterization of renal cell carcinoma-associated constitutional chromosome abnormalities by genome sequencing.
    Smith PS, Whitworth J, West H, Cook J, Gardiner C, Lim DHK, Morrison PJ, Hislop RG, Murray E, NIHR Rare Disease BioResourceNIHR BioResource, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge, UK., Tischkowitz M, Warren AY, Woodward ER, Maher ER.
    Genes Chromosomes Cancer; 2020 Jun; 59(6):333-347. PubMed ID: 31943436
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  • 28. Renal cell carcinoma with X;1 translocation in a child with Klinefelter syndrome.
    Yenamandra A, Zhou X, Trinchitella L, Susin M, Sastry S, Mehta L.
    Am J Med Genet; 1998 May 26; 77(4):281-4. PubMed ID: 9600736
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  • 29. Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13 approximately q22 breakpoints.
    Bodmer D, Janssen I, Jonkers Y, van den Berg E, Dijkhuizen T, Debiec-Rychter M, Schoenmakers E, van Kessel AG.
    Cancer Genet Cytogenet; 2002 Jul 15; 136(2):95-100. PubMed ID: 12237231
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  • 31. Mapping of the gene encoding the integrin-linked kinase, ILK, to human chromosome 11p15.5-p15.4.
    Hannigan GE, Bayani J, Weksberg R, Beatty B, Pandita A, Dedhar S, Squire J.
    Genomics; 1997 May 15; 42(1):177-9. PubMed ID: 9177792
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  • 32. Mapping of 29 YAC clones and identification of 3 YACs spanning the translocation t(3;8)(p14.2;q24.1) breakpoint at 8q24.1 in hereditary renal cell carcinoma.
    Shi G, Cannizzaro LA.
    Cytogenet Cell Genet; 1996 May 15; 75(2-3):180-5. PubMed ID: 9040788
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  • 35. Chromosome 1 analysis in chromophobe renal cell carcinomas with tissue microarray (TMA)-facilitated fluorescence in situ hybridization (FISH) demonstrates loss of 1p/1 which is also present in renal oncocytomas.
    Meyer PN, Cao Y, Jacobson K, Krausz T, Flanigan RC, Picken MM.
    Diagn Mol Pathol; 2008 Sep 15; 17(3):141-4. PubMed ID: 18382368
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  • 36. Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer.
    Koski TA, Lehtonen HJ, Jee KJ, Ninomiya S, Joosse SA, Vahteristo P, Kiuru M, Karhu A, Sammalkorpi H, Vanharanta S, Lehtonen R, Edgren H, Nederlof PM, Hietala M, Aittomäki K, Herva R, Knuutila S, Aaltonen LA, Launonen V.
    Genes Chromosomes Cancer; 2009 Jul 15; 48(7):544-51. PubMed ID: 19373782
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  • 37. Cytogenetic alterations in renal tumors: a study of 38 Southeast Asian patients.
    Lau LC, Tan PH, Chong TW, Foo KT, Yip S.
    Cancer Genet Cytogenet; 2007 May 15; 175(1):1-7. PubMed ID: 17498551
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