Showing results (1-10 of 9) with videos related to
Sort By:
Pageof 1
Prenatal Diagnosis|May 19, 2007
Clinical evaluation of isolated nonvisualized fetal gallbladderYifat Ochshorn, Guy Rosner, Dalit Barel, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|August 16, 2018
Whole-exome sequencing in fetuses with central nervous system abnormalitiesAdi Reches, Liran Hiersch, Sharon Simchoni, et al.Molecular Genetics and Metabolism|September 30, 2023
A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescueAlina Kurolap, Dalit Barel, Nava Shaul Lotan, et al.Journal of Pediatric Hematology/Oncology|September 3, 2004
Prenatal diagnosis in Li-Fraumeni syndromeSmadar Avigad, Dan Peleg, Dalit Barel, et al.Journal of Neurology|April 16, 2024
Genetic diagnosis and detection rates using C9orf72 repeat expansion and a multi-gene panel in amyotrophic lateral sclerosisDalit Barel, Daphna Marom, Penina Ponger, et al.Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|November 9, 2023
Telemedicine Versus Traditional In-Person Consultations: Comparison of Patient Satisfaction RatesUri Hamiel, Audelia Eshel Fuhrer, Nitsan Landau, et al.Movement Disorders Clinical Practice|June 5, 2025
High Genetic Diagnostic Yield for Patients with Rare Movement Disorders at a Single-Center Neurogenetics ClinicDvir Penn, Yam Amir, Gil Ben David, et al.European Journal of Neurology|June 23, 2026
A Practice Framework for Genetic Testing in Asymptomatic Relatives of Patients With Creutzfeldt-Jakob Disease: Experience and Insights From IsraelDror Shir, Noa Bregman, Aya Bar David, et al.Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.Pageof 1