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Yael Goldberg

Showing results (71-80 of 116) with videos related to

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Familial Cancer|April 5, 2008
Mutation spectrum in HNPCC in the Israeli populationYael Goldberg, Rinnat M Porat, Inbal Kedar, et al.
Neurology. Genetics|March 25, 2021
Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of WolframinAdi Wilf-Yarkoni, Oded Shor, Avi Fellner, et al.
Harefuah|July 2, 2023
[GENOTYPE-PHENOTYPE CORRELATIONS BY SPECIFIC FOUNDER VARIANTS IN BRCA IN ISRAELI WOMEN]Rachel Michaelson-Cohen, Yael Laitman, Inbal Kedar, et al.
Familial Cancer|November 9, 2020
Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factorsYael Laitman, Rachel Michaelson-Cohen, Rakefet Chen-Shtoyerman, et al.
Familial Cancer|October 24, 2009
An Ashkenazi founder mutation in the MSH6 gene leading to HNPCCYael Goldberg, Rinnat M Porat, Inbal Kedar, et al.
Familial Cancer|June 14, 2017
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in IsraelNaim Abu Freha, Yaara Leibovici Weissman, Alexander Fich, et al.
Journal of Medical Genetics|September 11, 2019
Paediatric systemic lupus erythematosus as a manifestation of constitutional mismatch repair deficiencyHelen Toledano, Naama Orenstein, Efrat Sofrin, et al.
Frontiers in Neurology|November 17, 2025
Expanding the spectrum of white matter abnormalities in Wolfram syndrome: a retrospective reviewJustin Simo, Heather M Lugar, Elka Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2019
Characterization of splice-altering mutations in inherited predisposition to cancerSilvia Casadei, Suleyman Gulsuner, Brian H Shirts, et al.
Journal of Medical Genetics|March 13, 2019
Homozygosity for CHEK2 p.Gly167Arg leads to a unique cancer syndrome with multiple complex chromosomal translocations in peripheral blood karyotypeTamar Paperna, Nitzan Sharon-Shwartzman, Alina Kurolap, et al.
Pageof 12

Showing results (71-80 of 116) with videos related to

Sort By:
Pageof 12
Familial Cancer|April 5, 2008
Mutation spectrum in HNPCC in the Israeli populationYael Goldberg, Rinnat M Porat, Inbal Kedar, et al.
Neurology. Genetics|March 25, 2021
Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of WolframinAdi Wilf-Yarkoni, Oded Shor, Avi Fellner, et al.
Harefuah|July 2, 2023
[GENOTYPE-PHENOTYPE CORRELATIONS BY SPECIFIC FOUNDER VARIANTS IN BRCA IN ISRAELI WOMEN]Rachel Michaelson-Cohen, Yael Laitman, Inbal Kedar, et al.
Familial Cancer|November 9, 2020
Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factorsYael Laitman, Rachel Michaelson-Cohen, Rakefet Chen-Shtoyerman, et al.
Familial Cancer|October 24, 2009
An Ashkenazi founder mutation in the MSH6 gene leading to HNPCCYael Goldberg, Rinnat M Porat, Inbal Kedar, et al.
Familial Cancer|June 14, 2017
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in IsraelNaim Abu Freha, Yaara Leibovici Weissman, Alexander Fich, et al.
Journal of Medical Genetics|September 11, 2019
Paediatric systemic lupus erythematosus as a manifestation of constitutional mismatch repair deficiencyHelen Toledano, Naama Orenstein, Efrat Sofrin, et al.
Frontiers in Neurology|November 17, 2025
Expanding the spectrum of white matter abnormalities in Wolfram syndrome: a retrospective reviewJustin Simo, Heather M Lugar, Elka Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2019
Characterization of splice-altering mutations in inherited predisposition to cancerSilvia Casadei, Suleyman Gulsuner, Brian H Shirts, et al.
Journal of Medical Genetics|March 13, 2019
Homozygosity for CHEK2 p.Gly167Arg leads to a unique cancer syndrome with multiple complex chromosomal translocations in peripheral blood karyotypeTamar Paperna, Nitzan Sharon-Shwartzman, Alina Kurolap, et al.
Pageof 12