Comparing the Efficiency of Three Protocols in Isolation of Cell Free Fetal DNA From Maternal Blood

por Karami, Fatemeh, Noori Daloii, Mohammad Reza, Hantooshzadeh, Seddigheh, Modarressi, Mohammad Hossein
Publicado 2017

A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients

por Jalilian, Nazanin, Tabatabaiefar, Mohammad Amin, Yazdanpanah, Mahboubeh, Darabi, Elham, Bahrami, Tayyeb, Zekri, Ali, Noori-Daloii, Mohammad Reza
Publicado 2018

Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report

por Sobhani, Maryam, Tabatabaiefar, Mohammad Amin, Ghafouri-Fard, Soudeh, Rajab, Asadollah, Hojjat, Asal, Kajbafzadeh, Abdol-Mohammad, Noori-Daloii, Mohammad Reza
Publicado 2020

Correction to: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report

por Sobhani, Maryam, Tabatabaiefar, Mohammad Amin, Ghafouri-Fard, Soudeh, Rajab, Asadollah, Hojjat, Asal, Kajbafzadeh, Abdol-Mohammad, Noori-Daloii, Mohammad Reza
Publicado 2020

Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations

por KOOHIYAN, Mahbobeh, REIISI, Somayeh, AZADEGAN-DEHKORDI, Fatemeh, SALEHI, Mansoor, ABTAHI, Hamidreza, HASHEMZADEH-CHALESHTORI, Morteza, NOORI-DALOII, Mohammad Reza, TABATABAIEFAR, Mohammad Amin
Publicado 2019

Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus

por Saee-Rad, Samira, Hashemi, Hassan, Miraftab, Mohammad, Noori-Daloii, Mohammad Reza, Chaleshtori, Morteza Hashemzadeh, Raoofian, Reza, Jafari, Fatemeh, Greene, Wayne, Fakhraie, Ghasem, Rezvan, Farhad, Heidari, Mansour
Publicado 2011