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Cancer Genetics and Cytogenetics|March 1, 1989
Involvement of chromosome 22 in a Merkel cell carcinoma in a patient with a previous meningiomaF Shabtai, A Sternberg, D Klar, et al.
Clinical Genetics|June 1, 1985
Familial syndrome with some features of the Langer-Giedion syndrome, and paracentric inversion of chromosome 8, inv 8 (q11.23----q21.1)F Shabtai, U Sandowski, R Nissimov, et al.
The Journal of Urology|September 1, 1991
Chromosomal anomaly and malformation syndrome with abdominal polyorchidismF Shabtai, A Schwartz, J Hart, et al.
Urologia Internationalis|January 1, 1985
Concomitance of urogenital with lymphoid and intestinal malignancies: more than a coincidenceF Shabtai, D Lask, D Kimchi, et al.
Human Genetics|January 1, 1979
Pure trisomy 17p in 60% cellsF Shabtai, A Shalev, J Chemke, et al.
Cancer Genetics and Cytogenetics|July 1, 1983
Marker chromosomes in a family with high incidence of cancerF Shabtai, D Klar, A Schwartz, et al.
Clinical Genetics|December 1, 1984
New anomalies found in the 11q-syndromeL Sirota, F Shabtai, I Landman, et al.
Cancer Genetics and Cytogenetics|January 15, 1985
Cytogenetic study of patients with carcinoma of the colon and rectum: particular C-band variants as possible markers for cancer pronenessF Shabtai, E Antebi, D Klar, et al.
Human Genetics|January 1, 1983
A new familial "fragile site" on chromosome 16 (q23-24). Cytogenetic and clinical considerationsF Shabtai, D Klar, R Nissimov, et al.
Anticancer Research|July 1, 1984
Juxta-centromeric fragility of chromosomes 1, 2, 9, 16, and immunodeficiency. Special reference to the fragility of chromosome 2 and its oncogenic potentialF Shabtai, D Klar, D Kimchi, et al.
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