Author = Majid Fardaei
Number of Articles: 4
1. Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles

Articles in Press, Accepted Manuscript, Available Online from 10 July 2019

Jafar Fallahi; Zahra Anvar; Vahid Razban; Mozhdeh Momtahan; Bahia Namavar-Jahromi; Majid Fardaei


2. Segmental Duplications as a Complement Strategy to Short Tandem Repeats in the Prenatal Diagnosis of Down Syndrome

Volume 44, Issue 3, May 2019, Pages 214-219

Mohammad Reza Miri; Jamileh Saberzadeh; Abbas Behzad Behbahani; Mohammad Bagher Tabei; Mohsen Alipour; Majid Fardaei


3. The First Case of a Small Supernumerary Marker Chromosome 18 in a Klinefelter Fetus: A Case Report

Volume 44, Issue 1, January 2019, Pages 65-69

Jamileh Saberzadeh; Mohammad Reza Miri; Mehdi Dianatpour; Abbas Behzad Behbahani; Mohammad Bagher Tabei; Mohsen Alipour; Mohammad Ali Faghihi; Majid Fardaei


4. MSX1 Mutation in Witkop Syndrome; A Case Report

Volume 38, June Supplement 2013, January 2013, Pages 191-194

Majid Fardaei; Faezeh Ghaderi; Somaye Hekmat; Reza Ghaderi