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Boleslaw Goldman

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Journal of Assisted Reproduction and Genetics|March 4, 2010
The single cell as a tool for genetic testing: credibility, precision, implicationKeren Dotan, Baruch Feldman, Boleslaw Goldman, et al.
Muscle & Nerve|June 18, 2003
Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosisVivian E Drory, Miriam Birnbaum, Leah Peleg, et al.
Human Genetics|January 17, 2004
Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesisAmos Frisch, Roberto Colombo, Elena Michaelovsky, et al.
Neurogenetics|December 3, 2003
Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestorMazal Karpati, Ephraim Gazit, Boleslaw Goldman, et al.
Journal of Neurosurgery|January 28, 2003
Comparative genomic hybridization analysis of craniopharyngiomasShlomit Rienstein, Eric F Adams, David Pilzer, et al.
American Journal of Medical Genetics. Part A|December 28, 2002
True hermaphroditism with ambiguous genitalia due to a complicated mosaic karyotype: clinical features, cytogenetic findings, and literature reviewDalit Modan-Moses, Talia Litmanovitch, Shlomit Rienstein, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 13, 2005
Genotyping of patients with sporadic and radiation-associated meningiomasSiegal Sadetzki, Pazit Flint-Richter, Sigal Starinsky, et al.
American Journal of Medical Genetics|September 5, 2002
Genetic counseling in hereditary breast/ovarian cancer in Israel: psychosocial impact and retention of genetic informationMichal DiCastro, Moshe Frydman, Irit Friedman, et al.
Gynecologic Oncology|September 19, 2003
Familial vs sporadic ovarian tumors: characteristic genomic alterations analyzed by CGHOfir Israeli, Walter H Gotlieb, Eitan Friedman, et al.
The Israel Medical Association Journal : IMAJ|March 6, 2002
Bloom syndrome and Fanconi's anemia: rate and ethnic origin of mutation carriers in IsraelLeah Peleg, Rachel Pesso, Boleslaw Goldman, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Assisted Reproduction and Genetics|March 4, 2010
The single cell as a tool for genetic testing: credibility, precision, implicationKeren Dotan, Baruch Feldman, Boleslaw Goldman, et al.
Muscle & Nerve|June 18, 2003
Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosisVivian E Drory, Miriam Birnbaum, Leah Peleg, et al.
Human Genetics|January 17, 2004
Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesisAmos Frisch, Roberto Colombo, Elena Michaelovsky, et al.
Neurogenetics|December 3, 2003
Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestorMazal Karpati, Ephraim Gazit, Boleslaw Goldman, et al.
Journal of Neurosurgery|January 28, 2003
Comparative genomic hybridization analysis of craniopharyngiomasShlomit Rienstein, Eric F Adams, David Pilzer, et al.
American Journal of Medical Genetics. Part A|December 28, 2002
True hermaphroditism with ambiguous genitalia due to a complicated mosaic karyotype: clinical features, cytogenetic findings, and literature reviewDalit Modan-Moses, Talia Litmanovitch, Shlomit Rienstein, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 13, 2005
Genotyping of patients with sporadic and radiation-associated meningiomasSiegal Sadetzki, Pazit Flint-Richter, Sigal Starinsky, et al.
American Journal of Medical Genetics|September 5, 2002
Genetic counseling in hereditary breast/ovarian cancer in Israel: psychosocial impact and retention of genetic informationMichal DiCastro, Moshe Frydman, Irit Friedman, et al.
Gynecologic Oncology|September 19, 2003
Familial vs sporadic ovarian tumors: characteristic genomic alterations analyzed by CGHOfir Israeli, Walter H Gotlieb, Eitan Friedman, et al.
The Israel Medical Association Journal : IMAJ|March 6, 2002
Bloom syndrome and Fanconi's anemia: rate and ethnic origin of mutation carriers in IsraelLeah Peleg, Rachel Pesso, Boleslaw Goldman, et al.
Pageof 2