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Cancer Genetics and Cytogenetics|July 1, 1988
New common fragile sitesF Hecht, E H Tajara, D Lockwood, et al.
Human Genetics|March 12, 1976
9p trisomy identified by Giemsa-11H E Wyandt, F Hecht, R E Magenis, et al.
Human Molecular Genetics|May 16, 1998
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site inductionM M Le Beau, F V Rassool, M E Neilly, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1998
A novel amplicon at 8p22-23 results in overexpression of cathepsin B in esophageal adenocarcinomaS J Hughes, T W Glover, X X Zhu, et al.
Human Molecular Genetics|November 1, 1995
Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper effluxJ Camakaris, M J Petris, L Bailey, et al.
Genes, Chromosomes & Cancer|December 1, 1994
Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3BF L Boldog, B Waggoner, T W Glover, et al.
Blood|June 1, 1978
Clonal evolution in atypical chronic granulocytic leukemia: a non-Philadelphia translocationG C Bagby, B Kaiser-McCaw, F Hecht, et al.
Genomics|February 1, 1990
Chromosome localization of human ARH genes, a ras-related gene familyL A Cannizzaro, P Madaule, F Hecht, et al.
Cancer Genetics and Cytogenetics|January 15, 1985
Histiocytic lymphoma cell lines: immunologic and cytogenetic studiesB K Hecht, A L Epstein, C S Berger, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 6, 2002
A confirmatory factor analysis of the WISC-III in a clinical sample with cross-validation in the standardization sampleD B Burton, A Sepehri, F Hecht, et al.
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