The library will be closed between August 10, 2026 and August 16, 2026. During this period, it will be possible to upload publications, but all other services will be suspended.
Ghalamkari, S.,
Mianesaz, H.,
Chitsaz, A.,
Ghazavi, M.,
Salehi, M.:
Proband-Only Exome Sequencing for Intellectual Disability in Iran: Diagnostic Yield and Genetic Insights.
Am. J. Med. Genet. A. 197 (4), 1-9, (article identifier: 63915), 2024.
Mianesaz, H.,
Ghalamkari, S.,
Salehi, M.,
Behnam, M.,
Hosseinzadeh, M.,
Basiri, K.,
Ghasemi, M.,
Sedghi, M.,
Ansari, B.:
Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants.
Molec Gen & Gen Med. 11 (2), 1-14, (article identifier: 2101), 2023.
Ghalamkari, S.,
Alavi, S.,
Mianesaz, H.,
Khosravian, F.,
Bahreini, A.,
Salehi, M.:
A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domain.
Life Sci. 269, 1-7, (article identifier: 118759), 2021.
Q1
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Q1
Medicine (miscellaneous)
D1
Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
2018
6.
Ghalamkari, S.,
Khosravian, F.,
Mianesaz, H.,
Kazemi, M.,
Behjati, M.,
Hakimian, S. M.,
Salehi, M.:
A Comparison Between Full-COLD PCR/HRM and PCR Sequencing for Detection of Mutations in Exon 9 of PIK3CA in Breast Cancer Patients.
Appl. Biochem. Biotechnol. 187 (3), 975-983, 2018.
