检索结果 - Brothman, A R

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  1. 1
    Benign copy number changes in clinical cytogenetic diagnostics by array CGH

    Benign copy number changes in clinical cytogenetic diagnostics by array CGH 由 Whitby, H., Tsalenko, A., Aston, E., Tsang, P., Mitchell, S., Bayrak-Toydemir, P., Hopkins, C., Peters, G., Bailey, D.K., Bruhn, L., Brothman, A.R.

    出版 2009
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    Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.

    Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients. 由 Lowery, M C, Morris, C A, Ewart, A, Brothman, L J, Zhu, X L, Leonard, C O, Carey, J C, Keating, M, Brothman, A R

    出版 1995
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    Allelic loss detected on chromosomes 8, 10, and 17 by fluorescence in situ hybridization using single-copy P1 probes on isolated nuclei from paraffin-embedded prostate tumors.

    Allelic loss detected on chromosomes 8, 10, and 17 by fluorescence in situ hybridization using single-copy P1 probes on isolated nuclei from paraffin-embedded prostate tumors. 由 Deubler, D. A., Williams, B. J., Zhu, X. L., Steele, M. R., Rohr, L. R., Jensen, J. C., Stephenson, R. A., Changus, J. E., Miller, G. J., Becich, M. J., Brothman, A. R.

    出版 1997
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