Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yuval Yaron

Showing results (41-50 of 122) with videos related to

Pageof 13
Sort By:
Prenatal Diagnosis|December 20, 2008
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?Adi Reches, Mira Malcov, Dalit Ben-Yosef, et al.
Brain : a Journal of Neurology|July 8, 2022
Methodological drawbacks in the alleged association between foetal sonographic anomalies and autismLena Sagi-Dain, Boaz Weisz, Karina Haratz Krajden, et al.
Human Mutation|September 27, 2002
MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndromeYuval Yaron, Bruria Ben Zeev, Ruth Shomrat, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|April 22, 2004
Feasibility of nuchal translucency in triplet pregnanciesSharon Maslovitz, Yuval Yaron, Gideon Fait, et al.
Fetal Diagnosis and Therapy|February 5, 2005
Nomograms for the sonographic measurement of the fetal philtrum and chinIlan Gull, Igal Wolman, Paul Merlob, et al.
Obstetrics and Gynecology|April 30, 2002
Third-trimester unexplained intrauterine fetal death is associated with inherited thrombophiliaAriel Many, Ronit Elad, Yuval Yaron, 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 aneuploidyRachel Michaelson-Cohen, Ruth Gershoni-Baruch, Reuven Sharoni, et al.
Cancer Genetics and Cytogenetics|February 28, 2003
Combined cytogenetic and array-based comparative genomic hybridization analyses of Wilms tumors: amplification and overexpression of the multidrug resistance associated protein 1 gene (MRP1) in a metachronous tumorMyriam Goldstein, Hanna Rennert, Anat Bar-Shira, et al.
Fetal Diagnosis and Therapy|August 23, 2005
Preimplantation genetic diagnosis of Canavan diseaseYuval Yaron, Tamar Schwartz, Nava Mey-Raz, et al.
Prenatal Diagnosis|April 25, 2007
Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended familyAdi Reches, Yuval Yaron, Kathryn Burdon, et al.
Pageof 13

Showing results (41-50 of 122) with videos related to

Sort By:
Pageof 13
Prenatal Diagnosis|December 20, 2008
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?Adi Reches, Mira Malcov, Dalit Ben-Yosef, et al.
Brain : a Journal of Neurology|July 8, 2022
Methodological drawbacks in the alleged association between foetal sonographic anomalies and autismLena Sagi-Dain, Boaz Weisz, Karina Haratz Krajden, et al.
Human Mutation|September 27, 2002
MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndromeYuval Yaron, Bruria Ben Zeev, Ruth Shomrat, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|April 22, 2004
Feasibility of nuchal translucency in triplet pregnanciesSharon Maslovitz, Yuval Yaron, Gideon Fait, et al.
Fetal Diagnosis and Therapy|February 5, 2005
Nomograms for the sonographic measurement of the fetal philtrum and chinIlan Gull, Igal Wolman, Paul Merlob, et al.
Obstetrics and Gynecology|April 30, 2002
Third-trimester unexplained intrauterine fetal death is associated with inherited thrombophiliaAriel Many, Ronit Elad, Yuval Yaron, 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 aneuploidyRachel Michaelson-Cohen, Ruth Gershoni-Baruch, Reuven Sharoni, et al.
Cancer Genetics and Cytogenetics|February 28, 2003
Combined cytogenetic and array-based comparative genomic hybridization analyses of Wilms tumors: amplification and overexpression of the multidrug resistance associated protein 1 gene (MRP1) in a metachronous tumorMyriam Goldstein, Hanna Rennert, Anat Bar-Shira, et al.
Fetal Diagnosis and Therapy|August 23, 2005
Preimplantation genetic diagnosis of Canavan diseaseYuval Yaron, Tamar Schwartz, Nava Mey-Raz, et al.
Prenatal Diagnosis|April 25, 2007
Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended familyAdi Reches, Yuval Yaron, Kathryn Burdon, et al.
Pageof 13