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Reeval Segel

Showing results (21-30 of 54) with videos related to

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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.
Journal of Perinatal Medicine|May 30, 2018
Chromosomal microarray findings in pregnancies with an isolated pelvic kidneyLena Sagi-Dain, Amihood Singer, Ayala Frumkin, et al.
American Journal of Human Genetics|September 8, 2009
Acute infantile liver failure due to mutations in the TRMU geneAvraham Zeharia, Avraham Shaag, Orit Pappo, et al.
Neurology|March 31, 2015
Copy number variations in cryptogenic cerebral palsyReeval Segel, Hilla Ben-Pazi, Sharon Zeligson, 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.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Obstetrics and Gynecology|November 7, 2018
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic AnomaliesLena Sagi-Dain, Idit Maya, Adi Reches, et al.
European Journal of Human Genetics : EJHG|June 1, 2010
New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the DanishDeborah J Morris-Rosendahl, Reeval Segel, A Peter Born, et al.
Endocrine|May 7, 2020
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSDFloris Levy-Khademi, Sharon Zeligson, Eran Lavi, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
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.
Journal of Perinatal Medicine|May 30, 2018
Chromosomal microarray findings in pregnancies with an isolated pelvic kidneyLena Sagi-Dain, Amihood Singer, Ayala Frumkin, et al.
American Journal of Human Genetics|September 8, 2009
Acute infantile liver failure due to mutations in the TRMU geneAvraham Zeharia, Avraham Shaag, Orit Pappo, et al.
Neurology|March 31, 2015
Copy number variations in cryptogenic cerebral palsyReeval Segel, Hilla Ben-Pazi, Sharon Zeligson, 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.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Obstetrics and Gynecology|November 7, 2018
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic AnomaliesLena Sagi-Dain, Idit Maya, Adi Reches, et al.
European Journal of Human Genetics : EJHG|June 1, 2010
New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the DanishDeborah J Morris-Rosendahl, Reeval Segel, A Peter Born, et al.
Endocrine|May 7, 2020
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSDFloris Levy-Khademi, Sharon Zeligson, Eran Lavi, et al.
Pageof 6