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Pediatric Endocrinology Reviews : PER
|
November 7, 2015
Chromosomal Microarray Analysis (CMA) a Clinical Diagnostic Tool in the Prenatal and Postnatal Settings
Nurit Assia Batzir, Mordechai Shohat, Idit Maya
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 deletions
Idit 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 pregnancies
Lena Sagi-Dain, Lina Basel-Salmon, Idit Maya
Bioethics
|
December 19, 2014
Prenatal screening: current practice, new developments, ethical challenges
Antina de Jong, Idit Maya, Jan M M van Lith
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.
Obstetrics and Gynecology
|
March 27, 2019
In Reply
Lena Sagi-Dain, Idit Maya, Amihood 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 setting
Idit 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 testing
Idit Maya, Rivka Sukenik-Halevy, Lina Basel-Salmon, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 18, 2015
A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysis
Aviva Mimouni-Bloch, Josepha Yeshaya, Sarit Kahana, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
Pediatric Endocrinology Reviews : PER
|
November 7, 2015
Chromosomal Microarray Analysis (CMA) a Clinical Diagnostic Tool in the Prenatal and Postnatal Settings
Nurit Assia Batzir, Mordechai Shohat, Idit Maya
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 deletions
Idit 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 pregnancies
Lena Sagi-Dain, Lina Basel-Salmon, Idit Maya
Bioethics
|
December 19, 2014
Prenatal screening: current practice, new developments, ethical challenges
Antina de Jong, Idit Maya, Jan M M van Lith
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.
Obstetrics and Gynecology
|
March 27, 2019
In Reply
Lena Sagi-Dain, Idit Maya, Amihood 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 setting
Idit 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 testing
Idit Maya, Rivka Sukenik-Halevy, Lina Basel-Salmon, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 18, 2015
A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysis
Aviva Mimouni-Bloch, Josepha Yeshaya, Sarit Kahana, et al.
Page
of 7