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

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

Neurodegenerative disorder and diffuse brain calcifications due to FARSB mutation in two siblings

por Karimzadeh, Parvaneh, Rezakhani, Sepideh, Miryounesi, Mohammad, Alijanpour, Sahar
Publicado 2022

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

Report of a Case with Trisomy 9 Mosaicism

por Miryounesi, Mohammad, Dianatpour, Mehdi, Shadmani, Zahra, Ghafouri-Fard, Soudeh
Publicado 2016

Homozygosity for a Robertsonian Translocation (13q;14q) in a Phenotypically Normal 44, XX Female with a History of Recurrent Abortion and a Normal Pregnancy Outcome

por Miryounesi, Mohammad, Diantpour, Mehdi, Motevaseli, Elahe, Ghafouri-Fard, Soudeh
Publicado 2016

Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees

por Ahmadloo, Somayeh, Talebi, Saeed, Miryounesi, Mohammad, Pasalar, Parvin, Keramatipour, Mohammad
Publicado 2016

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

An Iranian Congenital Adrenal Hypoplasia Patient with Elevated Testosterone in Infancy due to a Novel Pathogenic Frameshift Variant in NR0B1

por Kalayinia, Samira, Talebi, Saeed, Miryounesi, Mohammad, Sarkhail, Peymaneh, Mahdieh, Nejat
Publicado 2021

Co-culture of Mouse Embryonic Stem Cells with Sertoli Cells Promote in vitro Generation of Germ Cells

por Miryounesi, Mohammad, Nayernia, Karim, Dianatpour, Mahdi, Mansouri, Fatemeh, Modarressi, Mohammad Hossein
Publicado 2013

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

An immunocompetent patient with a nonsense mutation in NHEJ1 gene

por Esmaeilzadeh, Hossein, Bordbar, Mohammad Reza, Hojaji, Zahra, Habibzadeh, Parham, Afshinfar, Dorna, Miryounesi, Mohammad, Fardaei, Majid, Faghihi, Mohammad Ali
Publicado 2019

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

A vector-based system for the differentiation of mouse embryonic stem cells toward germ-line cells

por Ebrahimzadeh-Vesal, Reza, Shokrgozar, Mohammad Ali, Nayernia, Karim, Teimoori-Toolabi, Ladan, Miryounesi, Mohammad, Nourashrafeddin, Seyedmehdi, Ranji, Najmeh, Modarressi, Mohammad Hosein
Publicado 2014