Found: 12
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A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans–A cohort study.
- Published in:
- PLoS ONE, 2023, v. 18, n. 12, p. 1, doi. 10.1371/journal.pone.0294969
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- Publication type:
- Article
Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONOassociated X-linked syndromic intellectual developmental disorder.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1167054
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- Publication type:
- Article
De novo mutations in idiopathic male infertility—A pilot study.
- Published in:
- Andrology, 2021, v. 9, n. 1, p. 212, doi. 10.1111/andr.12897
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- Publication type:
- Article
Loss-of-Function Mutations in NR4A2 Cause Dopa-Responsive Dystonia Parkinsonism.
- Published in:
- 2020
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- Publication type:
- journal article
Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion.
- Published in:
- PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0196345
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- Publication type:
- Article
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.
- Published in:
- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0190601
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- Publication type:
- Article
A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion.
- Published in:
- American Journal of Reproductive Immunology, 2017, v. 78, n. 6, p. n/a, doi. 10.1111/aji.12765
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- Publication type:
- Article
Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 3, p. 365, doi. 10.1007/s10815-016-0848-4
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- Publication type:
- Article
The lack of association between angiotensin-converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis.
- Published in:
- Brain & Behavior, 2017, v. 7, n. 1, p. n/a, doi. 10.1002/brb3.600
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- Publication type:
- Article
Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion.
- Published in:
- Croatian Medical Journal, 2016, v. 57, n. 6, p. 566, doi. 10.3325/cmj.2016.57.566
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- Publication type:
- Article
The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2015, v. 32, n. 12, p. 1789, doi. 10.1007/s10815-015-0593-0
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- Publication type:
- Article
Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059220
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- Publication type:
- Article