Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of Cnksr2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (Mrxshg)
Alireza Biglari
Alireza Biglari

Professor of Genetics

Department Medical Genetics

School of Medicine

Tehran University of Medical Sciences

All Documents
17. Kh Domain Containing 3 Like (Khdc3l) Frame-Shift Mutation Causes Both Recurrent Pregnancy Loss and Hydatidiform Mole, European Journal of Obstetrics and Gynecology and Reproductive Biology (2021)