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Obstetrics and Gynecology
|
March 27, 2019
In Reply
Lena Sagi-Dain, Idit Maya, Amihood Singer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 15, 2023
Lessons learned from the first national population-based genetic carrier-screening program for Duchenne muscular dystrophy
Amihood Singer, Annemieke Aartsma-Rus, Julia Grinshpun-Cohen, et al.
Frontiers in Medicine
|
December 6, 2021
Trends in Non-invasive Prenatal Screening and Invasive Testing in Denmark (2000-2019) and Israel (2011-2019)
Lena Sagi-Dain, Amihood Singer, Olav B Petersen, et al.
Harefuah
|
December 18, 2024
[Letters to Editor: The risk for clinically significant copy number variants in pregnancies with two soft markers, Geriatriophobia - a new concept in the medical world in Israel]
Gustavo Malinger, Amihood Singer, Julia Grinshpun-Cohen, et al.
Breast Cancer Research and Treatment
|
April 14, 2019
Multigene panel testing in unselected Israeli breast cancer cases: mutational spectrum and use of BRCA1/2 mutation prediction algorithms
Rinat Bernstein-Molho, Amihood Singer, Yael Laitman, et al.
Neurogenetics
|
November 20, 2024
Dystrophinopathy patient data as a guide to interpretation of pregestational female population screening for DMD gene variants
Lena Sagi-Dain, Annemieke Aartsma-Rus, Moran Echar, et al.
Fetal Diagnosis and Therapy
|
August 21, 2014
Israeli Society of Medical Genetics NIPT Committee Opinion 072013: Non-invasive prenatal testing of cell-free DNA in maternal plasma for detection of fetal aneuploidy
Rachel Michaelson-Cohen, Ruth Gershoni-Baruch, Reuven Sharoni, et al.
American Journal of Obstetrics and Gynecology
|
May 30, 2021
The yield of chromosomal microarray in pregnancies with congenital cardiac defects and normal noninvasive prenatal screening
Lena Sagi-Dain, Amihood Singer, Reeval Segel, et al.
Brain : a Journal of Neurology
|
July 8, 2022
Methodological drawbacks in the alleged association between foetal sonographic anomalies and autism
Lena Sagi-Dain, Boaz Weisz, Karina Haratz Krajden, et al.
American Journal of Medical Genetics. Part A
|
July 8, 2017
Homozygous null variant in CRADD, encoding an adaptor protein that mediates apoptosis, is associated with lissencephaly
Tamar Harel, Nuphar Hacohen, Avraham Shaag, et al.
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Search research articles
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Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Obstetrics and Gynecology
|
March 27, 2019
In Reply
Lena Sagi-Dain, Idit Maya, Amihood Singer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 15, 2023
Lessons learned from the first national population-based genetic carrier-screening program for Duchenne muscular dystrophy
Amihood Singer, Annemieke Aartsma-Rus, Julia Grinshpun-Cohen, et al.
Frontiers in Medicine
|
December 6, 2021
Trends in Non-invasive Prenatal Screening and Invasive Testing in Denmark (2000-2019) and Israel (2011-2019)
Lena Sagi-Dain, Amihood Singer, Olav B Petersen, et al.
Harefuah
|
December 18, 2024
[Letters to Editor: The risk for clinically significant copy number variants in pregnancies with two soft markers, Geriatriophobia - a new concept in the medical world in Israel]
Gustavo Malinger, Amihood Singer, Julia Grinshpun-Cohen, et al.
Breast Cancer Research and Treatment
|
April 14, 2019
Multigene panel testing in unselected Israeli breast cancer cases: mutational spectrum and use of BRCA1/2 mutation prediction algorithms
Rinat Bernstein-Molho, Amihood Singer, Yael Laitman, et al.
Neurogenetics
|
November 20, 2024
Dystrophinopathy patient data as a guide to interpretation of pregestational female population screening for DMD gene variants
Lena Sagi-Dain, Annemieke Aartsma-Rus, Moran Echar, et al.
Fetal Diagnosis and Therapy
|
August 21, 2014
Israeli Society of Medical Genetics NIPT Committee Opinion 072013: Non-invasive prenatal testing of cell-free DNA in maternal plasma for detection of fetal aneuploidy
Rachel Michaelson-Cohen, Ruth Gershoni-Baruch, Reuven Sharoni, et al.
American Journal of Obstetrics and Gynecology
|
May 30, 2021
The yield of chromosomal microarray in pregnancies with congenital cardiac defects and normal noninvasive prenatal screening
Lena Sagi-Dain, Amihood Singer, Reeval Segel, et al.
Brain : a Journal of Neurology
|
July 8, 2022
Methodological drawbacks in the alleged association between foetal sonographic anomalies and autism
Lena Sagi-Dain, Boaz Weisz, Karina Haratz Krajden, et al.
American Journal of Medical Genetics. Part A
|
July 8, 2017
Homozygous null variant in CRADD, encoding an adaptor protein that mediates apoptosis, is associated with lissencephaly
Tamar Harel, Nuphar Hacohen, Avraham Shaag, et al.
Page
of 6