Gender determination in adults using calcaneal diameters from lateral foot X-ray images in the Iranian population

por Faress, Foroozan, Ameri, Maryam, Azizi, Hanieh, Saboori Shekofte, Hanieh, Hosseini, Rozita
Publicado 2021

A Novel Mutation in the OXCT1 Gene Causing Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Deficiency Starting with Neurologic Manifestations

por AMIRKASHANI, Davoud, ASADOLLAHI, Mostafa, HOSSEINI, Rozita, TALEBI, Saeed, GOLCHEHRE, Zahra, KERAMATIPOUR, Mohammad
Publicado 2023

Whole Exome Sequencing Reveals a XPNPEP3 Novel Mutation Causing Nephronophthisis in a Pediatric Patient

por Alizadeh, Rasoul, Jamshidi, Sanaz, Keramatipour, Mohammad, Moeinian, Parisa, Hosseini, Rozita, Otukesh, Hasan, Talebi, Saeed
Publicado 2020