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Fetal Diagnosis and Therapy|June 6, 2015
Nonvisualization of the Fetal Gallbladder: Can Levels of Gamma-Glutamyl Transpeptidase in Amniotic Fluid Predict Fetal Prognosis?Ron Bardin, Eran Ashwal, Bella Davidov, et al.Prenatal Diagnosis|July 1, 2006
Amniotic trisomy 11 mosaicism--is it a benign finding?Lina Basel-Vanagaite, Bella Davidov, Jane Friedman, et al.Genetic Testing and Molecular Biomarkers|December 26, 2013
The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestryDoron M Behar, Bella Davidov, Zippora Brownstein, et al.Gynecologic and Obstetric Investigation|March 6, 2026
Reference Range for Amniotic Fluid Bile Acids and Bilirubin in Uncomplicated PregnanciesDavid Danon, Asaf Romano, Orith Waisbourd-Zinman, et al.Prenatal Diagnosis|October 7, 2010
Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal settingIdit Maya, Bella Davidov, Liron Gershovitz, et al.European Journal of Human Genetics : EJHG|December 7, 2006
Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in IsraelLina Basel-Vanagaite, Ellen Taub, Gabrielle J Halpern, et al.Prenatal Diagnosis|October 4, 2024
Agenesis of the Ductus Venosus and Its Association With Genetic AbnormalitiesYarin Mash, Ron Bardin, Yinon Gilboa, et al.Clinical Genetics|March 22, 2022
Pathogenic variant-based preconception carrier screening in the Israeli Jewish populationBella Davidov, Amit Levon, Hadas Volkov, et al.European Journal of Human Genetics : EJHG|October 10, 2013
Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencingZippora Brownstein, Amal Abu-Rayyan, Daphne Karfunkel-Doron, et al.Molecular Genetics and Metabolism|December 15, 2015
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian originEyal Reinstein, Pola Smirin-Yosef, Irina Lagovsky, et al.Pageof 2