Commentary: Profiling of UGT1A1(*)6, UGT1A1(*)60, UGT1A1(*)93, and UGT1A1(*)28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing

por Heydari, Mohammad Reza, Fardaei, Majid
Publicado 2020

DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis

por Dastsooz, Hassan, Vahedi, Nazanin, Fardaei, Majid
Publicado 2013

A Novel Missense Mutation in CLCN1 Gene in a Family with Autosomal Recessive Congenital Myotonia

por Miryounesi, Mohammad, Ghafouri-Fard, Soudeh, Fardaei, Majid
Publicado 2016

Expression Analysis of Multiple Genes May Involve in Antimony Resistance among Leishmania major Clinical Isolates from Fars Province, Central Iran

por GHOBAKHLOO, Nafiseh, MOTAZEDIAN, Mohammad Hossein, FARDAEI, Majid
Publicado 2016

MSX1 Mutation in Witkop Syndrome; A Case Report

por Ghaderi, Faezeh, Hekmat, Somaye, Ghaderi, Reza, Fardaei, Majid
Publicado 2013

Mutation analysis of the CTNS gene in Iranian patients with infantile nephropathic cystinosis: identification of two novel mutations

por Sadeghipour, Forough, Basiratnia, Mitra, Derakhshan, Ali, Fardaei, Majid
Publicado 2017

Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren–Larsson Syndrome

por Taghdiri, Maryam, Kashef, Atie, Fardaei, Majid, Miryounesi, Mohammad
Publicado 2017

Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene

por Fardaei, Majid, Sarrafzadeh, Shaghayegh, Ghafouri-Fard, Soudeh, Miryounesi, Mohammad
Publicado 2015

The association between FTO rs9939609 gene polymorphism and anthropometric indices in adults

por Mehrdad, Mahsa, Fardaei, Majid, Fararouei, Mohammad, Eftekhari, Mohammad Hassan
Publicado 2020

Limb Girdle Muscular Dystrophy Type 2E Due to a Novel Large Deletion in SGCB Gene

por GHAFOURI-FARD, Soudeh, HASHEMI-GORJI, Feyzollah, FARDAEI, Majid, MIRYOUNESI, Mohammad
Publicado 2017

The Effect of Short-term Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) Diet on Hunger Hormones, Anthropometric Parameters, and Brain Structures in Middle-aged...

por Arjmand, Golnaz, Abbas-Zadeh, Mojtaba, Fardaei, Majid, Eftekhari, Mohammad Hassan
Publicado 2022

Novel mutation in the MED23 gene for intellectual disability: A case report and literature review

por Hashemi‐Gorji, Feyzollah, Fardaei, Majid, Tabei, Seyed Mohammad Bagher, Miryounesi, Mohammad
Publicado 2019

VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran

por Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid
Publicado 2017

Does the c.-273T>C variant in the upstream region of the HBB gene cause a thalassemia phenotype?

por Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Dehghanian, Fatemeh, Kamgarpour, Fatemeh, Fardaei, Majid
Publicado 2017

Author's Reply

por Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid
Publicado 2018

Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXA

por Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Kamgarpour, Fatemeh, Dehghanian, Fatemeh, Fardaei, Majid
Publicado 2018

Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports

por Dastsooz, Hassan, Nemati, Hamid, Fard, Mohammad Ali Farazi, Fardaei, Majid, Faghihi, Mohammad Ali
Publicado 2017

Association of FTO rs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults

por Mehrdad, Mahsa, Doaei, Saeid, Gholamalizadeh, Maryam, Fardaei, Majid, Fararouei, Mohammad, Eftekhari, Mohammad Hassan
Publicado 2020

Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles

por Fallahi, Jafar, Anvar, Zahra, Razban, Vahid, Momtahan, Mozhdeh, Namavar-Jahromi, Bahia, Fardaei, Majid
Publicado 2020

Multiplex ARMS PCR to Detect 8 Common Mutations of ATP7B Gene in Patients With Wilson Disease

por Dastsooz, Hassan, Imanieh, Mohammad Hadi, Dehghani, Seyed Mohsen, Haghighat, Mahmood, Moini, Maryam, Fardaei, Majid
Publicado 2013