Publications by authors named "Samira Behroozi"

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Bioinformatics analysis identifies dysregulation of miR-548F-3p and its hub gene in triple-negative breast cancer.
Samira Behroozi, Mahdieh Salimi, Najaf Allahyari Fard

Iran J Basic Med Sci· January 2025

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Next-generation sequencing approach to molecular diagnosis of Iranian patients with Duchenne/Becker muscular dystrophy: Several novel variants identified.
MohammadKazem Bakhshandeh, Samira Behroozi

eNeurologicalSci· March 2023

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A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss.
Hossein Fahimi, Samira Behroozi, Sadaf Noavar, Farshid Parvini

BMC Med Genomics· February 2021

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A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature.
Sadaf Noavar, Samira Behroozi, Taraneh Tatarcheh, Farshid Parvini, Majid Foroutan

BMC Med Genet· August 2019

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