Resultats de la cerca - Pinkel, D

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  1. 1

    Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. per Pinkel, D, Straume, T, Gray, J W

    Publicat a Proc Natl Acad Sci U S A (1986)
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    Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. per Pinkel, D, Landegent, J, Collins, C, Fuscoe, J, Segraves, R, Lucas, J, Gray, J

    Publicat a Proc Natl Acad Sci U S A (1988)
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    Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization. per Kallioniemi, A, Kallioniemi, O P, Piper, J, Tanner, M, Stokke, T, Chen, L, Smith, H S, Pinkel, D, Gray, J W, Waldman, F M

    Publicat a Proc Natl Acad Sci U S A (1994)
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    ERBB2 amplification in breast cancer analyzed by fluorescence in situ hybridization. per Kallioniemi, O P, Kallioniemi, A, Kurisu, W, Thor, A, Chen, L C, Smith, H S, Waldman, F M, Pinkel, D, Gray, J W

    Publicat a Proc Natl Acad Sci U S A (1992)
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    E2A deficiency leads to abnormalities in alphabeta T-cell development and to rapid development of T-cell lymphomas. per Bain, G, Engel, I, Robanus Maandag, E C, te Riele, H P, Voland, J R, Sharp, L L, Chun, J, Huey, B, Pinkel, D, Murre, C

    Publicat a Mol Cell Biol (1997)
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