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PUBMED FOR HANDHELDS

Journal Abstract Search


126 related items for PubMed ID: 3152871

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  • 23. Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization.
    Fabris V, Lamb CA, Keck C, Aldaz CM, Merani S, Lanari C.
    Cancer Genet Cytogenet; 2003 Apr 01; 142(1):36-45. PubMed ID: 12660031
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  • 25. Frequent hypomethylation in Wilms tumors of pericentromeric DNA in chromosomes 1 and 16.
    Qu GZ, Grundy PE, Narayan A, Ehrlich M.
    Cancer Genet Cytogenet; 1999 Feb 01; 109(1):34-9. PubMed ID: 9973957
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  • 27. Induction, processing and persistence of radiation-induced chromosomal aberrations involving hamster euchromatin and heterochromatin.
    Puerto S, Marcos R, Ramírez MJ, Creus A, Boei JJ, Meijers M, Natarajan AT, Surrallés J.
    Mutat Res; 2000 Sep 20; 469(2):169-79. PubMed ID: 10984678
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  • 32. Classification of X-ray-induced Robertsonian fusion-like configurations in mouse splenocytes.
    Boei JJ, Natarajan AT.
    Int J Radiat Biol; 1996 Apr 20; 69(4):421-7. PubMed ID: 8627124
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  • 34. Identification by C-banding of two human prostate tumour cell lines, 1013L and DU 145.
    Hartley-Asp B, Billström A, Kruse E.
    Int J Cancer; 1989 Jul 15; 44(1):161-4. PubMed ID: 2744886
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  • 38. Cytogenetic studies of esophageal carcinoma cell lines.
    Whang-Peng J, Banks-Schlegel SP, Lee EC.
    Cancer Genet Cytogenet; 1990 Mar 15; 45(1):101-20. PubMed ID: 2302677
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  • 40. Three-way and two-way rearrangements involving chromosomes 10, 2, 5 and 5, 2 in two marker chromosomes of a human melanoma cell line.
    Doneda L, Wiegant J, Larizza L.
    Melanoma Res; 1994 Aug 15; 4(4):259-65. PubMed ID: 7950361
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