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Cancer Genetics and Cytogenetics|April 1, 1988
Rhabdomyosarcoma in Roberts syndromeS L Wenger, J Blatt, M W Steele, et al.
Cancer Genetics and Cytogenetics|March 1, 1988
Familial fragile 8q22 involved as a cancer breakpoint in cells of a large bowel tumorF Shabtai, A Sternberg, D Klar, et al.
Cancer Genetics and Cytogenetics|October 1, 1987
Clonal chromosomal abnormalities in cutaneous T-cell lymphomaP E Shapiro, D Warburton, C L Berger, et al.
Cancer Genetics and Cytogenetics|December 1, 1986
Cytogenetic evidence for clonal evolution in B-cell chronic lymphocytic leukemiaT Han, K Ohtaki, N Sadamori, et al.
Cancer Genetics and Cytogenetics|September 1, 1986
Cytogenetic abnormalities in noncutaneous peripheral T-cell lymphomaW G Sanger, D D Weisenburger, J O Armitage, et al.
Cancer Genetics and Cytogenetics|January 1, 1991
Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probesM Kiechle-Schwarz, H J Decker, C S Berger, et al.
Cancer Genetics and Cytogenetics|May 1, 1990
Cancer in ataxia-telangiectasia patientsF Hecht, B K Hecht
Cancer Genetics and Cytogenetics|November 1, 1990
Mucoepidermoid tumor of the parotid gland showing a translocation (3;8)(p21;q12) and a deletion (5)(q22) as sole chromosome abnormalitiesJ Bullerdiek, M Vollrath, C Wittekind, et al.
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