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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: zeinali r, zeinali s. Front Genet. 2023 May 18;14:1140034. doi: 10.3389/fgene.2023.1140034. eCollection 2023. Front Genet. 2023. PMID: 37274793 Free PMC article.
Heterogeneity of hemoglobin h disease in childhood.
Zeinali S, Fallah MS, Bagherian H. Zeinali S, et al. N Engl J Med. 2011 May 26;364(21):2070-1; author reply 2071. doi: 10.1056/NEJMc1103406. N Engl J Med. 2011. PMID: 21612484 No abstract available.
A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect.
Davoudi-Dehaghani E, Zeinali S, Mahdieh N, Shirkavand A, Bagherian H, Tabatabaiefar MA. Davoudi-Dehaghani E, et al. Among authors: zeinali s. Int J Pediatr Otorhinolaryngol. 2013 May;77(5):821-6. doi: 10.1016/j.ijporl.2013.02.021. Epub 2013 Mar 21. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23523375
259 results