Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the Novel Dnmt3b Mutation in a Patient With Immunodeficiency, Centromeric Instability, and Facial Anomalies (Icf) Syndrome and a Bronchopulmonary Collateral Artery
Fatemeh Tahghighi
Fatemeh Tahghighi

Associate Professor of Pediatrics Rheumatology

Department Pediatrics

School of Medicine

Childrens Medical Center

Tehran University of Medical Sciences

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1. Post-Mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child, International Journal of Molecular and Cellular Medicine (2019)
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15. Post-Mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child, International Journal of Molecular and Cellular Medicine (2019)