Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the Novel Mutation C.7348C>T in Nf1 Gene Identified by Whole-Exome Sequencing in Patient With Overlapping Clinical Symptoms of Neurofibromatosis Type 1 and Bannayan–Riley–Ruvalcaba Syndrome
Mohamadreza Zarkesh
Mohamadreza Zarkesh

Associate Professor of Neonatal-Perinatal Medicine

Department Pediatrics

School of Medicine

Yas Hospital

Tehran University of Medical Sciences

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