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

od Heydari, Mohammad Reza, Fardaei, Majid
Wydane w Front Pediatr (2020)

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

od Dastsooz, Hassan, Vahedi, Nazanin, Fardaei, Majid
Wydane 2013

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

od Miryounesi, Mohammad, Ghafouri-Fard, Soudeh, Fardaei, Majid
Wydane w Iran J Med Sci (2016)

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

od GHOBAKHLOO, Nafiseh, MOTAZEDIAN, Mohammad Hossein, FARDAEI, Majid
Wydane w Iran J Parasitol (2016)

MSX1 Mutation in Witkop Syndrome; A Case Report

od Ghaderi, Faezeh, Hekmat, Somaye, Ghaderi, Reza, Fardaei, Majid
Wydane 2013

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

od Sadeghipour, Forough, Basiratnia, Mitra, Derakhshan, Ali, Fardaei, Majid
Wydane w Hum Genome Var (2017)

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

od Taghdiri, Maryam, Kashef, Atie, Fardaei, Majid, Miryounesi, Mohammad
Wydane w Clin Case Rep (2017)

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

od Fardaei, Majid, Sarrafzadeh, Shaghayegh, Ghafouri-Fard, Soudeh, Miryounesi, Mohammad
Wydane w Int J Mol Cell Med (2015)

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

od Mehrdad, Mahsa, Fardaei, Majid, Fararouei, Mohammad, Eftekhari, Mohammad Hassan
Wydane w J Physiol Anthropol (2020)

In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

od Fardaei, Majid, Larkin, Ken, Brook, J. David, Hamshere, Marion G.
Wydane 2001

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

od GHAFOURI-FARD, Soudeh, HASHEMI-GORJI, Feyzollah, FARDAEI, Majid, MIRYOUNESI, Mohammad
Wydane w Iran J Child Neurol (2017)

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

od Hashemi‐Gorji, Feyzollah, Fardaei, Majid, Tabei, Seyed Mohammad Bagher, Miryounesi, Mohammad
Wydane w Clin Case Rep (2019)

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

od Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid
Wydane w J Ophthalmic Vis Res (2017)

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

od Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Dehghanian, Fatemeh, Kamgarpour, Fatemeh, Fardaei, Majid
Wydane w Blood Res (2017)

Author's Reply

od Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid
Wydane w J Ophthalmic Vis Res (2018)

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

od Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Kamgarpour, Fatemeh, Dehghanian, Fatemeh, Fardaei, Majid
Wydane w Hum Genome Var (2018)

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

od Dastsooz, Hassan, Nemati, Hamid, Fard, Mohammad Ali Farazi, Fardaei, Majid, Faghihi, Mohammad Ali
Wydane w BMC Med Genet (2017)

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

od Mehrdad, Mahsa, Doaei, Saeid, Gholamalizadeh, Maryam, Fardaei, Majid, Fararouei, Mohammad, Eftekhari, Mohammad Hassan
Wydane w Adipocyte (2020)

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

od Fallahi, Jafar, Anvar, Zahra, Razban, Vahid, Momtahan, Mozhdeh, Namavar-Jahromi, Bahia, Fardaei, Majid
Wydane w Iran J Med Sci (2020)

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

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