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F Shabtai

Showing results (11-20 of 52) with videos related to

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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 Halbrecht
American Journal of Diseases of Children (1960)|May 1, 1972
Prune-belly syndrome with chromosomal fragmentI Halbrecht, L Komlos, F Shabtai
Clinical Genetics|January 1, 1985
Aneuploidy of chromosome X, variants 22 and fra(17p12)F Shabtai, J Hart, I Halbrecht
Human Genetics|January 1, 1980
The fragile site on chromosome 16 (q21q22). Data on four new familiesF Shabtai, S Bichacho, I Halbrecht
Journal 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.
Annales De Genetique|January 1, 1981
A new family with a satellited YF Shabtai, N Eilam, E Elian, et al.
American Journal of Medical Genetics|October 1, 1986
Interstitial 7q deletion [46,XY,del (7) (pter----cen::q112----qter)] in a retarded quadriplegic boy with normal beta glucuronidaseM Frydman, J Steinberger, F Shabtai, 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.
World Journal of Surgery|November 1, 1991
Cytogenetic studies in patients with gastric cancerJ Abarbanel, F Shabtai, S Kyzer, 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.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Annales De Genetique|January 1, 1982
Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31)F Shabtai, D Klar, I Halbrecht
American Journal of Diseases of Children (1960)|May 1, 1972
Prune-belly syndrome with chromosomal fragmentI Halbrecht, L Komlos, F Shabtai
Clinical Genetics|January 1, 1985
Aneuploidy of chromosome X, variants 22 and fra(17p12)F Shabtai, J Hart, I Halbrecht
Human Genetics|January 1, 1980
The fragile site on chromosome 16 (q21q22). Data on four new familiesF Shabtai, S Bichacho, I Halbrecht
Journal 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.
Annales De Genetique|January 1, 1981
A new family with a satellited YF Shabtai, N Eilam, E Elian, et al.
American Journal of Medical Genetics|October 1, 1986
Interstitial 7q deletion [46,XY,del (7) (pter----cen::q112----qter)] in a retarded quadriplegic boy with normal beta glucuronidaseM Frydman, J Steinberger, F Shabtai, 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.
World Journal of Surgery|November 1, 1991
Cytogenetic studies in patients with gastric cancerJ Abarbanel, F Shabtai, S Kyzer, 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.
Pageof 6