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

Novel LAMA2 Gene Mutations Associated with Merosin-Deficient Congenital Muscular Dystrophy

por Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza, Dashti, Parisa, Miryounesi, Mohammad
Publicado 2018

Association between single nucleotide polymorphisms rs12722489 and multiple sclerosis in Iranian patients with multiple sclerosis

por Ahmadi, Habib, Yassaee, Vahid Reza, Mirfakhraie, Reza, Hashemi-Gorji, Feyzollah
Publicado 2020

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

Association of a Novel Nonsense Mutation in KIAA1279 with Goldberg-Shprintzen Syndrome

por SALEHPOUR, Shadab, HASHEMI-GORJI, Feyzollah, SOLTANI, Ziba, GHAFOURI-FARD, Soudeh, MIRYOUNESI, Mohammad
Publicado 2017

First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population

por Soltani, Ziba, Karami, Fatemeh, Yassaee, Vahidreza, Hashemi Gorji, Feyzollah, Talebzadeh, Mahdieh, Miryounesi, Mohammad
Publicado 2016

A Novel Splice Site Mutation in HPS1 Gene is Associated with Hermansky-Pudlak Syndrome-1 (HPS1) in an Iranian Family

por Ghafouri-Fard, Soudeh, Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza, Alipour, Nasrin, Miryounesi, Mohammad
Publicado 2016

A Novel Nonsense Mutation in PANK2 Gene in Two Patients with Pantothenate Kinase-Associated Neurodegeneration

por Ghafouri-Fard, Soudeh, Yassaee, Vahid Reza, Rezayi, Alireza, Hashemi-Gorji, Feyzollah, Alipour, Nasrin, Miryounesi, Mohammad
Publicado 2016

Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

por Ravesh, Zeinab, Dianatpour, Mahdi, Fardaei, Majid, Taghdiri, Maryam, Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza, Miryounesi, Mohammad
Publicado 2018

BAX pro-apoptotic gene alterations in repeated pregnancy loss

por Mohammad Seyedhassani, Seyed, Houshmand, Massoud, Mehdi Kalantar, Seyed, Aflatoonian, Abbas, Modabber, Glayol, Hashemi-Gorji, Feyzollah, Hadipour, Zahra
Publicado 2011

Genetic Analysis of Iranian Patients with Familial Hypercholesterolemia

por Ekrami, Mahdis, Torabi, Maryam, Ghafouri-Fard, Soudeh, Mowla, Javad, Soltani, Bahram Mohammad, Hashemi-Gorji, Feyzollah, Mohebbi, Zahra, Miryounesi, Mohammad
Publicado 2018

Gene expression profiling of the 8q22-24 position in human breast cancer: TSPYL5, MTDH, ATAD2 and CCNE2 genes are implicated in oncogenesis, while WISP1 and EXT1 genes may predict...

por Taghavi, Afsoon, Akbari, Mohammad Esmaeil, Hashemi-Bahremani, Mohammad, Nafissi, Nahid, Khalilnezhad, Ahad, Poorhosseini, Seyed Mohammad, Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza
Publicado 2016