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Samira DabbaghBagheri

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SLC26A4 pathogenic variants as a third cause of hearing loss: Role of three exons in DFNB4 deafness in Iran

2019 Indian Journal of Otology
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Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia

2016 Indian Journal of Hematology and Blood Transfusion
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Homozygosity mapping and CDH23 mutation analysis in Iranian deaf families

2016 Hearing, Balance and Communication
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GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss

2015 European Archives of Oto-rhino-laryngology
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Citations (6)