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GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
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
Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia.
DabbaghBagheri S, Ghadami S, Mollazadeh F, Saadat A, Zeinali S.
DabbaghBagheri S, et al.
Indian J Hematol Blood Transfus. 2016 Dec;32(4):500-503. doi: 10.1007/s12288-016-0682-y. Epub 2016 May 26.
Indian J Hematol Blood Transfus. 2016.
PMID: 27812264
Free PMC article.
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Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility.
Bahrami Zadegan S, Dabbagh Bagheri S, Joudaki A, Samiee Aref MH, Saeidian AH, Abiri M, Zeinali S.
Bahrami Zadegan S, et al.
Andrologia. 2017 Dec 28. doi: 10.1111/and.12946. Online ahead of print.
Andrologia. 2017.
PMID: 29282760
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Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families.
Amirian A, Zafari Z, Dalili M, Saber S, Karimipoor M, Dabbagh Bagheri S, Fazelifar AF, Zeinali S.
Amirian A, et al.
J Arrhythm. 2018 Apr 16;34(3):286-290. doi: 10.1002/joa3.12042. eCollection 2018 Jun.
J Arrhythm. 2018.
PMID: 29951145
Free PMC article.
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First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variant.
Shojaei Z, Abiri M, Zafarghandi Motlagh F, Amini M, Dabbagh Bagheri S, Asnavandi S, Asadi S, Bagherian H, Zeinali S.
Shojaei Z, et al.
Blood Cells Mol Dis. 2024 Jan;104:102797. doi: 10.1016/j.bcmd.2023.102797. Epub 2023 Sep 29.
Blood Cells Mol Dis. 2024.
PMID: 37826942
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