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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

167 related items for PubMed ID: 7513608

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  • 24. Frequent allele loss on 9p21-22 defines a smallest common region in the vicinity of the CDKN2 gene in sporadic breast cancer.
    An HX, Niederacher D, Picard F, van Roeyen C, Bender HG, Beckmann MW.
    Genes Chromosomes Cancer; 1996 Sep; 17(1):14-20. PubMed ID: 8889502
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  • 26. Characterization of chromosome 9 in human ovarian neoplasia identifies frequent genetic imbalance on 9q and rare alterations involving 9p, including CDKN2.
    Schultz DC, Vanderveer L, Buetow KH, Boente MP, Ozols RF, Hamilton TC, Godwin AK.
    Cancer Res; 1995 May 15; 55(10):2150-7. PubMed ID: 7743516
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  • 31. Peculiar structure and location of 9p21 homozygous deletion breakpoints in human cancer cells.
    Florl AR, Schulz WA.
    Genes Chromosomes Cancer; 2003 Jun 15; 37(2):141-8. PubMed ID: 12696062
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  • 32. Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia.
    Coleman A, Fountain JW, Nobori T, Olopade OI, Robertson G, Housman DE, Lugo TG.
    Cancer Res; 1994 Jan 15; 54(2):344-8. PubMed ID: 8275465
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