Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the Hypotrichosis With Juvenile Macular Dystrophy: Combination of Whole-Genome Sequencing and Genome-Wide Homozygosity Mapping Identifies a Large Deletion in Cdh3 Initially Undetected by Whole-Exome Sequencing—A Lesson From Next-Generation Sequencing
Mehrzad Mehdizadeh
Mehrzad Mehdizadeh

Professor of Radiology

Department Radiology

School of Medicine

Childrens Medical Center

Pediatric Urology and Regenerative Medicine Research Center

Tehran University of Medical Sciences

All Documents
12. Joint Stiffness Leads to the Diagnosis of a Rare Disease, Iranian Journal of Pediatrics (2022)
22. Cerebral Aspergillosis, Archives of Iranian medicine (2019)
29. Caustic Agent Ingestion by a 1.5-Year-Old Boy, Acta Medica Iranica (2016)