Found: 13
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Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 4, p. 1, doi. 10.1002/mgg3.2421
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- Publication type:
- Article
Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect.
- Published in:
- 2020
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- Publication type:
- journal article
A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran.
- Published in:
- 2022
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- Publication type:
- journal article
Genetic study of a patient with congenital central hypoventilation syndrome in Iran: a case report.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 12, p. 8239, doi. 10.1007/s11033-021-06746-7
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- Publication type:
- Article
Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group.
- Published in:
- Journal of Molecular Neuroscience, 2016, v. 59, n. 3, p. 392, doi. 10.1007/s12031-016-0772-1
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- Publication type:
- Article
A Study on the CLCN5 Gene in Iranian Patients: A Report of Novel and Recurrent Mutations.
- Published in:
- Nephron, 2023, v. 147, n. 8, p. 470, doi. 10.1159/000528344
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- Publication type:
- Article
Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 12, p. N.PAG, doi. 10.1002/mgg3.1029
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- Publication type:
- Article
Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01016-y
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- Publication type:
- Article
Comparative Analysis of 198 SARS-CoV-2 Genomes from Iran and West Asia, February 2020 to December 2021.
- Published in:
- Iranian Journal of Pathology, 2023, v. 18, n. 3, p. 289, doi. 10.30699/IJP.2023.557658.2935
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- Publication type:
- Article
Bethlem myopathy: A novel homozygous variant of c.385C>T (p.Arg129Cys) in the COL6A2 gene.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Hints From the Cellular Functions to the Practical Outlook of Circular RNAs.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.679446
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- Publication type:
- Article
Sex-specific association of RANTES gene −403 variant in Meniere's disease.
- Published in:
- European Archives of Oto-Rhino-Laryngology, 2015, v. 272, n. 9, p. 2221, doi. 10.1007/s00405-014-3151-y
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- Publication type:
- Article