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Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.
Eur J Hum Genet. 2024 Jan 26. doi: 10.1038/s41431-024-01533-x. Online ahead of print.
Eur J Hum Genet. 2024.
PMID: 38278869
Reduction in circulating vitamin D binding protein in patients with multiple sclerosis.
Maghbooli Z, Omidifar A, Varzandi T, Salehnezhad T, Sahraian MA.
Maghbooli Z, et al. Among authors: salehnezhad t.
BMC Neurol. 2021 Apr 20;21(1):168. doi: 10.1186/s12883-021-02200-0.
BMC Neurol. 2021.
PMID: 33879066
Free PMC article.
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Expression assessment of a panel of long non-coding RNAs in gastric malignancy.
Esfandi F, Salehnezhad T, Taheri M, Afsharpad M, Hafez AA, Oskooei VK, Ghafouri-Fard S.
Esfandi F, et al. Among authors: salehnezhad t.
Exp Mol Pathol. 2020 Apr;113:104383. doi: 10.1016/j.yexmp.2020.104383. Epub 2020 Jan 23.
Exp Mol Pathol. 2020.
PMID: 31982396
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