Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

por Zardadi, Safoura, Rayat, Sima, Hassani Doabsari, Maryam, Keramatipour, Mohammad, Morovvati, Saeid
Publicado 2021

A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia

por Rahbaran, Marzieh, Hassani Doabsari, Maryam, Salavitabar, Simindokht, Mokhberian, Neda, Morovvati, Ziba, Morovvati, Saeid
Publicado 2019

PPARG (Pro12Ala) genetic variant and risk of T2DM: a systematic review and meta-analysis

por Sarhangi, Negar, Sharifi, Farshad, Hashemian, Leila, Hassani Doabsari, Maryam, Heshmatzad, Katayoun, Rahbaran, Marzieh, Jamaldini, Seyed Hamid, Aghaei Meybodi, Hamid Reza, Hasanzad, Mandana
Publicado 2020