Found: 21
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Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation.
- Published in:
- Iranian Journal of Basic Medical Sciences, 2011, v. 14, n. 3, p. 213
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- Publication type:
- Article
The genetic landscape and possible therapeutics of neurofibromatosis type 2.
- Published in:
- Cancer Cell International, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12935-023-02940-8
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- Publication type:
- Article
Emotion Regulation Training on Irritability, Alexithymia, and Interpersonal Problems of Adolescents With Disruptive Mood Dysregulation Disorder.
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- Journal of Research & Health, 2023, v. 13, n. 6, p. 427, doi. 10.32598/JRH.13.6.2202.1
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- Publication type:
- Article
Alginate/chitosan hydrogel containing olfactory ectomesenchymal stem cells for sciatic nerve tissue engineering.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 9, p. 15357, doi. 10.1002/jcp.28183
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- Publication type:
- Article
Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01287-9
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- Publication type:
- Article
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.
- Published in:
- Human Genetics, 2007, v. 121, n. 1, p. 43, doi. 10.1007/s00439-006-0292-0
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- Publication type:
- Article
Novel phenotype and genotype spectrum of NARS2 and literature review of previous mutations.
- Published in:
- Irish Journal of Medical Science, 2022, v. 191, n. 4, p. 1877, doi. 10.1007/s11845-021-02736-7
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- Publication type:
- Article
How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us.
- Published in:
- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 13, p. 5869, doi. 10.1111/jcmm.16610
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- Publication type:
- Article
Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01682-w
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- Publication type:
- Article
Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01682-w
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- Publication type:
- Article
The Anticipation and Inheritance Pattern of c.487A>G Mutation in the GJB2 Gene.
- Published in:
- Archives of Iranian Medicine (AIM), 2012, v. 15, n. 1, p. 49
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- Publication type:
- Article
Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population.
- Published in:
- BMC Cardiovascular Disorders, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12872-022-02695-6
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- Publication type:
- Article
Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population.
- Published in:
- 2022
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- Publication type:
- journal article
Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage.
- Published in:
- Journal of Clinical Laboratory Analysis, 2023, v. 37, n. 21/22, p. 1, doi. 10.1002/jcla.24983
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- Publication type:
- Article
Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T‐ARMS‐PCR assay.
- Published in:
- Journal of Clinical Laboratory Analysis, 2022, v. 36, n. 1, p. 1, doi. 10.1002/jcla.24150
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- Publication type:
- Article
A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian family.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 8, p. 1976, doi. 10.1002/ajmg.a.34077
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- Publication type:
- Article
Prediction of Imposter Syndrome in Gifted Female Students based on Ego Development, Self-efficacy, and Self-awareness.
- Published in:
- International Journal of Behavioral Sciences, 2023, v. 17, n. 2, p. 57, doi. 10.30491/IJBS.2023.360222.1849
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- Publication type:
- Article
Association of genetic variations in the mitochondrial DNA control region with presbycusis.
- Published in:
- Clinical Interventions in Aging, 2017, v. 12, p. 459, doi. 10.2147/CIA.S123278
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- Publication type:
- Article
Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment.
- Published in:
- Clinical Interventions in Aging, 2016, v. 11, p. 1003, doi. 10.2147/CIA.S109110
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- Publication type:
- Article
The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis.
- Published in:
- Therapeutics & Clinical Risk Management, 2016, v. 12, p. 1573, doi. 10.2147/TCRM.S117491
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- Publication type:
- Article
Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss.
- Published in:
- 2016
- By:
- Publication type:
- journal article