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Identification of Two Novel Mutations in the ATM Gene from Patients with Ataxia-Telangiectasia by Whole Exome Sequencing.
Curr Genomics. 2019 Nov;20(7):531-534. doi: 10.2174/1389202920666191107153734.
Curr Genomics. 2019.
PMID: 32655291
Free PMC article.
Association of a novel homozygous mutation in the HMGCS2 gene with an HMGCSD in an Iranian patient.
Heidari M, Soleyman-Nejad M, Isazadeh A, Shapouri J, Taskhiri MH, Ahangari R, Mohamadi AR, Ebrahimi M, Karimi H, Bolhassani M, Karimi Z, Heidari M.
Heidari M, et al. Among authors: soleyman nejad m.
Mol Genet Genomic Med. 2020 Nov;8(11):e1507. doi: 10.1002/mgg3.1507. Epub 2020 Sep 23.
Mol Genet Genomic Med. 2020.
PMID: 32969201
Free PMC article.
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Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing.
Heidari M, Soleyman-Nejad M, Isazadeh A, Taskiri MH, Bolhassani M, Sadighi N, Shiri Z, Karimi Z, Heidari M.
Heidari M, et al. Among authors: soleyman nejad m.
Iran J Basic Med Sci. 2021 Feb;24(2):191-195. doi: 10.22038/IJBMS.2020.44487.10405.
Iran J Basic Med Sci. 2021.
PMID: 33953858
Free PMC article.
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Identification of Two Novel Mutations in PKHD1 Gene from Two Families with Polycystic Kidney Disease by Whole Exome Sequencing.
Heidari M, Gharshasbi H, Isazadeh A, Soleyman-Nejad M, Taskhiri MH, Shapouri J, Bolhassani M, Sadighi N, Heidari M.
Heidari M, et al. Among authors: soleyman nejad m.
Curr Genomics. 2021 Oct 18;22(3):232-236. doi: 10.2174/1389202922666210219111810.
Curr Genomics. 2021.
PMID: 34975292
Free PMC article.
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Prevalence of Chromosomal Abnormalities in Iranian Patients with Infertility.
Abbaspour S, Isazadeh A, Heidari M, Heidari M, Hajazimian S, Soleyman-Nejad M, Taskhiri MH, Bolhassani M, Ebrahimi AH, Keshavarz P, Shiri Z, Heidari M.
Abbaspour S, et al. Among authors: soleyman nejad m.
Arch Iran Med. 2023 Feb 1;26(2):110-116. doi: 10.34172/aim.2023.17.
Arch Iran Med. 2023.
PMID: 37543931
Free PMC article.
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Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII.
Ebrahimi AH, Bolhassani M, Zarei MR, Heidari M, ArdeshirDavani A, Mehrtash AH, Shiri Z, Heidari M, Soleyman-Nejad M, Taskhiri MH, Norouzbeigi A, Heidari M.
Ebrahimi AH, et al. Among authors: soleyman nejad m.
Arch Iran Med. 2024 Apr 1;27(4):223-226. doi: 10.34172/aim.2024.32.
Arch Iran Med. 2024.
PMID: 38685849
Free article.
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