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Acta Geneticae Medicae Et Gemellologiae|January 1, 1977
Triple mosaicism with two autosomally unbalanced cell lines in a phenotypically normal oligospermic manF Shabtai, S Bichacho, I HalbrechtHuman Genetics|January 1, 1980
The fragile site on chromosome 16 (q21q22). Data on four new familiesF Shabtai, S Bichacho, I HalbrechtActa Geneticae Medicae Et Gemellologiae|January 1, 1978
Cytogenetic observations in infertile men working with insecticidal compoundsF Shabtai, S Bichacho, I HalbrechtAmerican Journal of Medical Genetics|May 1, 1988
Fragile X expression in Martin-Bell syndrome, intellectually normal individuals, and neoplasia, interpreted by a viral hypothesisF Shabtai, J Hart, D Klar, et al.Human Genetics|January 1, 1987
Alpha-interferon and fragility at 16q22. A study on 15 selected controls and 146 selected patientsF Shabtai, J Orlyn, J Hart, et al.Human Genetics|January 1, 1983
Familial fragility on chromosome 16 (fra 16q22) enhanced by both interferon and Distamycin AF Shabtai, D Klar, S Bichacho, et al.Clinical Genetics|January 1, 1979
Risk of malignancy and chromosomal polymorphism: a possible mechanism of associationF Shabtai, I HalbrechtActa Geneticae Medicae Et Gemellologiae|January 1, 1975
An unusual case of hemoglobin Bart's hydrops fetalisI Halbrecht, F ShabtaiCancer Genetics and Cytogenetics|January 1, 1981
Studies of banded chromosomes in patients with acute lymphocytic leukemia, including one patient with the Burkitt-type (L3)F Shabtai, I HalbrechtActa Geneticae Medicae Et Gemellologiae|January 1, 1977
Primary amenorrhea with a new mosaic 46,XXqi/47,XXqi Xp-. Consideration on the X isochromosome formation and X chromosome inactivationI Halbrecht, F Shabtai, C KuperstainPageof 9