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Cancer Genetics and Cytogenetics|April 1, 1983
Fibrous histiocytoma cell line: chromosome studies of mouse and manF Hecht, C Berger, B K Hecht, et al.Cancer Genetics and Cytogenetics|March 15, 1986
The Philadelphia chromosome: a model of cancer and molecular cytogeneticsA A Sandberg, R M Gemmill, B K Hecht, et al.The American Journal of Medicine|June 1, 1984
Chromosome analysis in hematologic disorders. The leukemiasA A Sandberg, R Morgan, C Berger, et al.Cancer Genetics and Cytogenetics|September 1, 1982
Translocations involving chromosomes #3 and #12: hematologic diseases associated with abnormalities of these chromosomesA A Sandberg, B K Hecht, S M Ondreyco, et al.American Journal of Medical Genetics|November 1, 1993
Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literatureH A Hales, C M Peterson, J Carey, et al.Cancer Genetics and Cytogenetics|March 15, 1986
Chromosome clues to acute leukemia in Down's syndromeF Hecht, B K Hecht, R Morgan, et al.Cancer Genetics and Cytogenetics|March 1, 1983
Adenocarcinoma of the gallbladder: chromosome abnormalities in a genetic form of cancerF Hecht, D J Kuban, C Berger, et al.Cancer Genetics and Cytogenetics|July 1, 1988
Regional chromosome localization of human papillomavirus integration sites near fragile sites, oncogenes, and cancer chromosome breakpointsL A Cannizzaro, M Dürst, M J Mendez, et al.Cancer Genetics and Cytogenetics|January 1, 1985
The Philadelphia (Ph) chromosome in leukemia. II. Variant Ph translocations in acute lymphoblastic leukemiaA A Sandberg, R Morgan, T J Kipps, et al.Cancer Genetics and Cytogenetics|July 1, 1988
New common fragile sitesF Hecht, E H Tajara, D Lockwood, et al.Pageof 14