Found: 7
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Effect of inbreeding on intellectual disability revisited by trio sequencing.
- Published in:
- Clinical Genetics, 2019, v. 95, n. 1, p. 151, doi. 10.1111/cge.13463
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- Article
Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière's Disease.
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- Archives of Iranian Medicine (AIM), 2020, v. 23, n. 5, p. 319, doi. 10.34172/aim.2020.21
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- Article
Carrier Testing in Known Autosomal Recessive Intellectual Disability Genes in an Iranian Healthy Individual Using Exome Sequencing.
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- Archives of Iranian Medicine (AIM), 2015, v. 18, n. 10, p. 643, doi. 0151810/AIM.006
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- Article
Distinct genetic variation and heterogeneity of the Iranian population.
- Published in:
- PLoS Genetics, 2019, v. 15, n. 9, p. 1, doi. 10.1371/journal.pgen.1008385
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- Article
Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-86309-9
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- Article
Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease.
- Published in:
- Medical Principles & Practice, 2015, v. 24, n. 4, p. 351, doi. 10.1159/000430842
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- Article
Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families.
- Published in:
- Journal of Genetics, 2015, v. 94, n. 3, p. 483, doi. 10.1007/s12041-015-0537-6
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- Article