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Annales De Genetique|January 1, 1982
Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31)F Shabtai, D Klar, I HalbrechtJournal of Pediatric Ophthalmology and Strabismus|July 1, 1980
Leber's optic neuropathy--a cytogenetic study of a familyR Avisar, F Shabtai, I Halbrecht, et al.Cancer Genetics and Cytogenetics|September 1, 1985
On the meaning of fragile sites in cancer risk and developmentF Shabtai, D Klar, J Hart, et al.Human Genetics|July 1, 1986
Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22)F Shabtai, J Hart, D Klar, 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.Journal of Cancer Research and Clinical Oncology|January 1, 1980
New complex Ph' translocation t (10; 14; 22) in bone marrow cells and in PHA-stimulated peripheral blood cultures in chronic myelocytic leukaemiaF Shabtai, U Gafter, S Weiss, et al.Journal of Medical Genetics|June 1, 1979
Triple mosaicism 45,XY,--18/46, XY/47,XY,+18M Frydman, F Shabtai, Y Barak, et al.Mutation Research|June 1, 1990
Ca antagonist verapamil and tumor promoter 12-O-tetradecanoylphorbol-13- acetate (TPA) induce chromosomal aberrations in human lymphocytesJ Friedman, F Shabtai, U Sandowski, et al.Cancer Genetics and Cytogenetics|July 1, 1987
Inversion (16)(p13q22) in tumor cells of sigmoid colonF Shabtai, A Sternberg, D Klar, et al.Pageof 9