Author = Farkhondeh Behjati
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies

Volume 21, Issue 3, June 2019, Pages 337-349

10.22074/cellj.2019.6053

Akbar Mohammadzadeh; Susan Akbaroghli; Ehsan Aghaei-Moghadam; Nejat Mahdieh; Reza Shervin Badv; Payman Jamali; Roxana Kariminejad; Zahra Chavoshzadeh; Saghar Ghasemi Firouzabadi; Roxana Mansour Ghanaie; Ahoura Nozari; Sussan Banihashemi; Fatemeh Hadipour; Zahra Hadipour; Ariana Kariminejad; Hossein Najmabadi; Yousef Shafeghati; Farkhondeh Behjati


A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family

Volume 21, Issue 1, November 2018, Pages 70-77

10.22074/cellj.2019.5734

Ahoura Nozari; Ehsan Aghaei-Moghadam; Aliakbar Zeinaloo; Afagh Alavi; Saghar Ghasemi Firouzabdi; Shohre Minaee; Marzieh Eskandari Hesari; Farkhondeh Behjati