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Showing results for
mohammad galehdari[au]
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Mohammad Galedari[au]
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A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family.
Mol Genet Genomic Med. 2020 Oct;8(10):e1413. doi: 10.1002/mgg3.1413. Epub 2020 Jul 22.
Mol Genet Genomic Med. 2020.
PMID: 32697043
Free PMC article.
Evaluation of GKN1 and GKN2 gene expression as a biomarker of gastric cancer.
Dokhaee F, Mazhari S, Galehdari M, Bahadori Monfared A, Baghaei K.
Dokhaee F, et al. Among authors: galehdari m.
Gastroenterol Hepatol Bed Bench. 2018 Winter;11(Suppl 1):S140-S145.
Gastroenterol Hepatol Bed Bench. 2018.
PMID: 30774821
Free PMC article.
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Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis.
Razmara E, Azimi H, Bitaraf A, Daneshmand MA, Galehdari M, Dokhanchi M, Esmaeilzadeh-Gharehdaghi E, Garshasbi M.
Razmara E, et al. Among authors: galehdari m.
Mol Genet Genomic Med. 2020 Mar;8(3):e1118. doi: 10.1002/mgg3.1118. Epub 2020 Jan 15.
Mol Genet Genomic Med. 2020.
PMID: 31944631
Free PMC article.
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A case report of congenital myasthenic syndrome caused by a mutation in theCHRNE genein the Iranian population.
Farjami Z, Khodaenia N, Ebrahimi N, Zamani G, Ashnaei AH, Galehdari M, Moradyar M, Houshmand M.
Farjami Z, et al. Among authors: galehdari m.
Iran J Child Neurol. 2020 Fall;14(4):87-94.
Iran J Child Neurol. 2020.
PMID: 33193787
Free PMC article.
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