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Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
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
GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
Zeinali S, Davoudi-Dehaghani E, Azadmehr S, DabbaghBagheri S, Bagherian H, Jamali M, Zafarghandimotlagh F, Masoodifard M, BandehiSarhaddi A, Rejali L, Sahebi S.
Zeinali S, et al. Among authors: azadmehr s.
Eur Arch Otorhinolaryngol. 2015 Sep;272(9):2255-9. doi: 10.1007/s00405-014-3171-7. Epub 2014 Jul 11.
Eur Arch Otorhinolaryngol. 2015.
PMID: 25012701
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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.
Arch Iran Med. 2021 Dec 1;24(12):887-896. doi: 10.34172/aim.2021.133.
Arch Iran Med. 2021.
PMID: 35014236
Free article.
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Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran.
Alimohammadi-Bidhendi S, Azadmehr S, Razipour M, Zeinali S, Eslami M, Davoudi-Dehaghani E.
Alimohammadi-Bidhendi S, et al. Among authors: azadmehr s.
Hemoglobin. 2021 Jan;45(1):37-40. doi: 10.1080/03630269.2021.1882482. Epub 2021 Mar 27.
Hemoglobin. 2021.
PMID: 33775199
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