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Page 1
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
Shirzadeh T, Saeidian AH, Bagherian H, Salehpour S, Setoodeh A, Alaei MR, Youssefian L, Samavat A, Touati A, Fallah MS, Vahidnezhad H, Karimipoor M, Azadmehr S, Raeisi M, Bandehi Sarhadi A, Zafarghandi Motlagh F, Jamali M, Zeinali Z, Abiri M, Zeinali S; Additional individual contributors. Shirzadeh T, et al. Among authors: zafarghandi motlagh f. J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29. J Inherit Metab Dis. 2018. PMID: 30159852
Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort.
Shafaat M, Alaee MR, Rahmanifar A, Setoodeh A, Razzaghy-Azar M, Bagherian H, Bagheri SD, Zafarghandi Motlagh F, Hashemi M, Abiri M, Zeinali S. Shafaat M, et al. Among authors: zafarghandi motlagh f. Metab Brain Dis. 2018 Oct;33(5):1689-1697. doi: 10.1007/s11011-018-0277-4. Epub 2018 Jul 18. Metab Brain Dis. 2018. PMID: 30022420
The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A.
Azadmehr S, Rahiminejad F, Zafarghandi Motlagh F, Jamali M, Ghazizadeh Tehrani P, Shirzadeh T, Bagherian H, Karimipoor M, Davoudi-Dehaghani E, Zeinali S. Azadmehr S, et al. Among authors: zafarghandi motlagh f. Arch Iran Med. 2021 Dec 1;24(12):887-896. doi: 10.34172/aim.2021.133. Arch Iran Med. 2021. PMID: 35014236 Free article.
Genetic attributes of Iranian cystic fibrosis patients: the diagnostic efficiency of CFTR mutations in over a decade.
Hosseini Nami A, Kabiri M, Zafarghandi Motlagh F, Shirzadeh T, Fakhari N, Karimi A, Bagherian H, Jamali M, Younesikhah S, Shadman S, Zeinali R, Zeinali S. Hosseini Nami A, et al. Among authors: zafarghandi motlagh f. Front Genet. 2023 May 18;14:1140034. doi: 10.3389/fgene.2023.1140034. eCollection 2023. Front Genet. 2023. PMID: 37274793 Free PMC article.
Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher Patients.
Sardarpour N, Bagherian H, Zafarghandi Motlagh F, Shirzadeh T, Asnavandi S, Younesikhah S, Salehpour S, Setoodeh A, Alaei MR, Zeinali S. Sardarpour N, et al. Among authors: zafarghandi motlagh f. Int J Mol Cell Med. 2023;12(1):40-50. doi: 10.22088/IJMCM.BUMS.12.1.40. Int J Mol Cell Med. 2023. PMID: 37942259 Free PMC article.