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International Journal of Pediatric Otorhinolaryngology|July 9, 2010
High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 geneNejat Mahdieh, Hamideh Bagherian, Atefeh Shirkavand, et al.Protein Expression and Purification|August 14, 2017
Rapid characterization of the CHO platform cell line and identification of pseudo attP sites for PhiC31 integraseNarges Damavandi, Mozhgan Raigani, Atefeh Joudaki, et al.Hemoglobin|December 5, 2009
A novel polymorphism causes a different restriction pattern by RsaI in the beta-globin gene cluster: application in prenatal diagnosisAtefeh Valaei, Fatemeh Bayat, Alireza Kordafshari, et al.Hemoglobin|July 30, 2011
β-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, IranMohammad Saeid Rahiminejad, Sirous Zeinali, Abdolreza Afrasiabi, et al.Metabolic Brain Disease|June 26, 2019
Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutationsMehdi Shafaat, Mehrdad Hashemi, Ahmad Majd, et al.Scientific Reports|January 18, 2023
Aberrant promoter hypermethylation of miR-335 and miR-145 is involved in breast cancer PD-L1 overexpressionSara Hajibabaei, Fattah Sotoodehnejadnematalahi, Nahid Nafissi, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 26, 2021
Identification of a novel mutation in congenital afibrinogenemia in Iranian patientsSomayeh Takrim Nojehdeh, Marzieh Mojbafan, Mahboobeh Masoodifard, et al.Acta Haematologica|April 25, 2008
Molecular analysis of factor IX gene in an Iranian female with severe hemophilia BMorteza Karimipoor, Leila Kokabee, Esmat Kamali, et al.Orphanet Journal of Rare Diseases|January 16, 2020
Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effectMarzieh Mojbafan, Reza Bahmani, Samira Dabbagh Bagheri, et al.Journal of Human Genetics|August 27, 2010
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populationsNejat Mahdieh, Bahareh Rabbani, Susan Wiley, et al.Pageof 18