Tehran University of Medical Sciences

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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
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)