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Tzvia Mann

Showing results (1-10 of 7) with videos related to

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Scientific Reports|November 17, 2021
Detection of single nucleotide and copy number variants in the Fabry disease-associated GLA gene using nanopore sequencingAlbina Nowak, Omer Murik, Tzvia Mann, et al.
Microbiology Spectrum|May 17, 2023
Whole-Genome Sequencing Reveals Differences among Kingella kingae Strains from Carriers and Patients with Invasive InfectionsOmer Murik, David A Zeevi, Tzvia Mann, et al.
Journal of Clinical and Experimental Hepatology|February 2, 2026
Markedly Low Prevalence of Fatty Liver Despite Obesity in Prader-Willi Syndrome: A Search for Protective Genetic MarkersOmer Murik, Varda Gross-Tsur, Tzvia Mann, et al.
Molecular Genetics and Genomics : MGG|April 29, 2022
Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangementsRachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, et al.
Scientific Reports|October 21, 2023
SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testingDaniel Backenroth, Gheona Altarescu, Fouad Zahdeh, et al.
Harefuah|March 9, 2026
[Resolving Genomic Mysteries with Long-read Sequencing]Omer Murik, David Zeevi, Tzvia Mann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testingDavid A Zeevi, Daniel Backenroth, Elinor Hakam-Spector, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Scientific Reports|November 17, 2021
Detection of single nucleotide and copy number variants in the Fabry disease-associated GLA gene using nanopore sequencingAlbina Nowak, Omer Murik, Tzvia Mann, et al.
Microbiology Spectrum|May 17, 2023
Whole-Genome Sequencing Reveals Differences among Kingella kingae Strains from Carriers and Patients with Invasive InfectionsOmer Murik, David A Zeevi, Tzvia Mann, et al.
Journal of Clinical and Experimental Hepatology|February 2, 2026
Markedly Low Prevalence of Fatty Liver Despite Obesity in Prader-Willi Syndrome: A Search for Protective Genetic MarkersOmer Murik, Varda Gross-Tsur, Tzvia Mann, et al.
Molecular Genetics and Genomics : MGG|April 29, 2022
Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangementsRachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, et al.
Scientific Reports|October 21, 2023
SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testingDaniel Backenroth, Gheona Altarescu, Fouad Zahdeh, et al.
Harefuah|March 9, 2026
[Resolving Genomic Mysteries with Long-read Sequencing]Omer Murik, David Zeevi, Tzvia Mann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testingDavid A Zeevi, Daniel Backenroth, Elinor Hakam-Spector, et al.
Pageof 1