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Lina Basel-Salmon

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European Journal of Human Genetics : EJHG|February 13, 2024
Phenotypic compatibility and specificity in genomic variant classificationLina Basel-Salmon
European Journal of Medical Genetics|December 24, 2021
Challenges in variant interpretation in prenatal exome sequencingLina Basel-Salmon, Rivka Sukenik-Halevy
Best Practice & Research. Clinical Obstetrics & Gynaecology|September 11, 2024
Fetal whole genome sequencing as a clinical diagnostic tool: Advantages, limitations and pitfallsLina Basel-Salmon, Dana Brabbing-Goldstein
Journal of Neurology|May 8, 2023
Ordering genetic testing by neurologists: points to considerAvi Fellner, Yael Goldberg, Lina Basel-Salmon
European Journal of Human Genetics : EJHG|March 23, 2021
Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletionsIdit Maya, Lina Basel-Salmon, Lena Sagi-Dain
American Journal of Obstetrics and Gynecology|December 19, 2021
Physician anxiety or maternal choice?Lena Sagi-Dain, Lina Basel-Salmon, Idit Maya
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Empowering informed choices: revisiting the discussion on prenatal genetic testing in all pregnanciesLena Sagi-Dain, Lina Basel-Salmon, Idit Maya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2020
High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?Idit Maya, Lina Basel-Salmon, Ami Singer, et al.
Acta Obstetricia Et Gynecologica Scandinavica|October 21, 2020
Ten points to consider when providing genetic counseling for variants of incomplete penetrance and variable expressivity detected in a prenatal settingIdit Maya, Rivka Sukenik-Halevy, Lina Basel-Salmon, et al.
Journal of Perinatal Medicine|May 19, 2023
A call for public funding of invasive and non-invasive prenatal testingIdit Maya, Rivka Sukenik-Halevy, Lina Basel-Salmon, et al.
Pageof 10

Showing results (1-10 of 96) with videos related to

Sort By:
Pageof 10
European Journal of Human Genetics : EJHG|February 13, 2024
Phenotypic compatibility and specificity in genomic variant classificationLina Basel-Salmon
European Journal of Medical Genetics|December 24, 2021
Challenges in variant interpretation in prenatal exome sequencingLina Basel-Salmon, Rivka Sukenik-Halevy
Best Practice & Research. Clinical Obstetrics & Gynaecology|September 11, 2024
Fetal whole genome sequencing as a clinical diagnostic tool: Advantages, limitations and pitfallsLina Basel-Salmon, Dana Brabbing-Goldstein
Journal of Neurology|May 8, 2023
Ordering genetic testing by neurologists: points to considerAvi Fellner, Yael Goldberg, Lina Basel-Salmon
European Journal of Human Genetics : EJHG|March 23, 2021
Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletionsIdit Maya, Lina Basel-Salmon, Lena Sagi-Dain
American Journal of Obstetrics and Gynecology|December 19, 2021
Physician anxiety or maternal choice?Lena Sagi-Dain, Lina Basel-Salmon, Idit Maya
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Empowering informed choices: revisiting the discussion on prenatal genetic testing in all pregnanciesLena Sagi-Dain, Lina Basel-Salmon, Idit Maya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2020
High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?Idit Maya, Lina Basel-Salmon, Ami Singer, et al.
Acta Obstetricia Et Gynecologica Scandinavica|October 21, 2020
Ten points to consider when providing genetic counseling for variants of incomplete penetrance and variable expressivity detected in a prenatal settingIdit Maya, Rivka Sukenik-Halevy, Lina Basel-Salmon, et al.
Journal of Perinatal Medicine|May 19, 2023
A call for public funding of invasive and non-invasive prenatal testingIdit Maya, Rivka Sukenik-Halevy, Lina Basel-Salmon, et al.
Pageof 10