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F Shabtai

Showing results (1-10 of 52) with videos related to

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Clinical Genetics|January 1, 1979
Risk of malignancy and chromosomal polymorphism: a possible mechanism of associationF Shabtai, I Halbrecht
Acta Geneticae Medicae Et Gemellologiae|January 1, 1975
An unusual case of hemoglobin Bart's hydrops fetalisI Halbrecht, F Shabtai
Cancer 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 Halbrecht
Hereditas|January 1, 1981
Interpretation of a marker chromosome 17p in multiple myelomaF Shabtai, I Halbrecht
Clinical Genetics|July 1, 1980
Bloom's syndrome, missing Y, hypogonadism and cancerF Shabtai, I Halbrecht
Acta 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 Kuperstain
Diseases of the Colon and Rectum|December 1, 1994
Chromosome sensitivity to bleomycin-induced mutagenesis in lymphocytes from colorectal cancer patients under 40 years of ageZ Fireman, F Shabtai, B Lurie
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 Halbrecht
Acta Geneticae Medicae Et Gemellologiae|January 1, 1978
Cytogenetic observations in infertile men working with insecticidal compoundsF Shabtai, S Bichacho, I Halbrecht
Human Genetics|January 1, 1982
Chromosome 17 has a real fragile site at p12F Shabtai, D Klar, I Halbrecht
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Clinical Genetics|January 1, 1979
Risk of malignancy and chromosomal polymorphism: a possible mechanism of associationF Shabtai, I Halbrecht
Acta Geneticae Medicae Et Gemellologiae|January 1, 1975
An unusual case of hemoglobin Bart's hydrops fetalisI Halbrecht, F Shabtai
Cancer 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 Halbrecht
Hereditas|January 1, 1981
Interpretation of a marker chromosome 17p in multiple myelomaF Shabtai, I Halbrecht
Clinical Genetics|July 1, 1980
Bloom's syndrome, missing Y, hypogonadism and cancerF Shabtai, I Halbrecht
Acta 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 Kuperstain
Diseases of the Colon and Rectum|December 1, 1994
Chromosome sensitivity to bleomycin-induced mutagenesis in lymphocytes from colorectal cancer patients under 40 years of ageZ Fireman, F Shabtai, B Lurie
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 Halbrecht
Acta Geneticae Medicae Et Gemellologiae|January 1, 1978
Cytogenetic observations in infertile men working with insecticidal compoundsF Shabtai, S Bichacho, I Halbrecht
Human Genetics|January 1, 1982
Chromosome 17 has a real fragile site at p12F Shabtai, D Klar, I Halbrecht
Pageof 6