Gholamreza Mohammadian

A novel COL7A1 gene mutation in an Iranian individual suffering dystrophic epidermolysis bullosa.

H. Galehdari, M. Pedram, B. Salehi, 2010, The Journal of molecular diagnostics : JMD.

Consultations in Molecular Diagnostics A Novel COL7A1 Gene Mutation in an Iranian Individual Suffering Dystrophic Epidermolysis Bullosa

H. Galehdari, M. Pedram, B. Salehi, 2010 .

A facile one-pot synthesis of substituted N-{[2-(aminocarbonyl)phenylamino]thioxomethyl}benzamides and 2-aryl-quinazolin-4(3H)-ones

R. Mohebat, M. Raja, Gholamreza Mohammadian, 2015, Russian Journal of General Chemistry.

An Efficient One‐Pot Synthesis of Bis‐1‐(aroyl)‐3‐(aryl)thiourea.

R. Mohebat, Gholamreza Mohammadian, 2013 .

Novel mutation in the EXT-1 gene in an Iranian family affected with hereditary multiple exostoses.

H. Galehdari, A. Foroughmand, M. Rasouli, 2008, Pakistan journal of biological sciences : PJBS.

The Prevalence of Inherited Microcephaly in Autosomal Recessive Diseases Resulted from Consanguineous Marriage in Ahvaz, Iran

A. Foroughmand, Z. Sadeghi, Gholamreza Mohammadian, 2016 .

Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran

H. Galehdari, A. Foroughmand, Maryam Naderi Soorki, 2009, Indian journal of human genetics.

Detection of a novel mutation in the GAA gene in an Iranian child with glycogen storage disease type II.

H. Galehdari, A. Khodadadi, M. Emami, 2013, Archives of Iranian medicine.