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Iran's Multiple Indicator Demographic and Health Survey - 2010: Study Protocol.
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- International Journal of Preventive Medicine, 2014, v. 5, n. 5, p. 632
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- Article
Role of ATP-Binding Cassette Transporters in the Chemoresistance of Anaplastic Thyroid Cancer: A Systematic Review.
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- Endocrinology, 2019, v. 160, n. 8, p. 2015, doi. 10.1210/en.2019-00241
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- Article
Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran.
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- Clinical Genetics, 2021, v. 100, n. 1, p. 59, doi. 10.1111/cge.13956
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- Article
Comprehensive genotype‐phenotype correlation in AP‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients.
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- Clinical Genetics, 2021, v. 99, n. 1, p. 187, doi. 10.1111/cge.13845
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- Article
Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families.
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- Clinical Genetics, 2019, v. 95, n. 6, p. 718, doi. 10.1111/cge.13549
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- Article
Effect of inbreeding on intellectual disability revisited by trio sequencing.
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- Clinical Genetics, 2019, v. 95, n. 1, p. 151, doi. 10.1111/cge.13463
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- Article
Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.
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- Iranian Biomedical Journal, 2016, v. 20, n. 4, p. 201, doi. 10.7508/ibj.2016.04.003
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- Article
CEP104 and CEP290; Genes with Ciliary Functions Cause Intellectual Disability in Multiple Families.
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- Archives of Iranian Medicine (AIM), 2021, v. 24, n. 5, p. 364, doi. 10.34172/aim.2021.53
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- Article
Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum.
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- Archives of Iranian Medicine (AIM), 2020, v. 23, n. 7, p. 426, doi. 10.34172/aim.2020.39
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- Article
Contribution of Iran in Elucidating the Genetic Causes of Autosomal Recessive Intellectual Disability.
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- Archives of Iranian Medicine (AIM), 2019, v. 22, n. 8, p. 461
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- Article
De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy.
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- Archives of Iranian Medicine (AIM), 2017, v. 20, n. 9, p. 617
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- Article
Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.
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- Archives of Iranian Medicine (AIM), 2016, v. 19, n. 10, p. 724
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- Article
Impact of Whole Exorne Sequencing among Iranian Patients with Autosomal Recessive Retinitis Pigmentosa.
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- Archives of Iranian Medicine (AIM), 2015, v. 18, n. 11, p. 776
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- Article
Distinct genetic variation and heterogeneity of the Iranian population.
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- PLoS Genetics, 2019, v. 15, n. 9, p. 1, doi. 10.1371/journal.pgen.1008385
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- Article
Genetic etiology of hearing loss in Iran.
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- Human Genetics, 2022, v. 141, n. 3/4, p. 623, doi. 10.1007/s00439-021-02421-w
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- Article
Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups.
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- Archives of Iranian Medicine (AIM), 2024, v. 27, n. 2, p. 79, doi. 10.34172/aim.2024.13
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- Article
Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian Cohort.
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- Archives of Iranian Medicine (AIM), 2023, v. 26, n. 4, p. 186, doi. 10.34172/aim.2023.29
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- Article
Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations.
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- Archives of Iranian Medicine (AIM), 2023, v. 26, n. 2, p. 69, doi. 10.34172/aim.2023.12
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- Article
Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability.
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- Archives of Iranian Medicine (AIM), 2022, v. 25, n. 12, p. 788, doi. 10.34172/aim.2022.124
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- Article
Targeted Next Generation Sequencing Revealed Novel Variants in the PKD1 and PKD2 Genes of Iranian Patients with Autosomal Dominant Polycystic Kidney Disease.
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- Archives of Iranian Medicine (AIM), 2022, v. 25, n. 9, p. 600, doi. 10.34172/aim.2022.95
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- Article
Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends.
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- Archives of Iranian Medicine (AIM), 2022, v. 25, n. 8, p. 508, doi. 10.34172/aim.2022.83
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- Article
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
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- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00393-0
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- Article
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
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- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00393-0
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- Article
Developing a household survey tool for health equity: A practical guide in Islamic Republic of Iran.
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- Medical Journal of the Islamic Republic of Iran, 2015, v. 29, p. 1
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- Article
Vaccination effects on reducing COVID‐19 complications in pregnancy: A large‐scale report from Iran.
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- International Journal of Gynecology & Obstetrics, 2023, v. 163, n. 3, p. 1012, doi. 10.1002/ijgo.15077
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- Article
Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations.
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- Journal of Genetics, 2016, v. 95, n. 3, p. 667, doi. 10.1007/s12041-016-0682-6
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- Article
COVID‐19 knowledge, attitudes, and practices among Iranian pregnant and postpartum women: A national study.
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- Journal of Obstetrics & Gynaecology Research, 2023, v. 49, n. 9, p. 2295, doi. 10.1111/jog.15724
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- Article
Iranome: A catalog of genomic variations in the Iranian population.
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- Human Mutation, 2019, v. 40, n. 11, p. 1968, doi. 10.1002/humu.23880
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- Article
Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients.
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- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 4, p. 1, doi. 10.1002/mgg3.1894
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- Article
Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1418
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- Article