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Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 1, p. 59, doi. 10.1111/cge.13956
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- Article
Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism.
- Published in:
- Archives of Iranian Medicine (AIM), 2020, v. 23, n. 12, p. 842, doi. 10.34172/aim.2020.112
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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
Targeted Next Generation Sequencing Revealed Novel Variants in the PKD1 and PKD2 Genes of Iranian Patients with Autosomal Dominant Polycystic Kidney Disease.
- Published in:
- Archives of Iranian Medicine (AIM), 2022, v. 25, n. 9, p. 600, doi. 10.34172/aim.2022.95
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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
PDZD7 and Hearing Loss: More Than Just a Modifier.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 2957, doi. 10.1002/ajmg.a.37274
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- Article