Works matching IS 03406717 AND DT 2017 AND VI 136 AND IP 6
Results: 11
Common genetic etiology between 'multiple sclerosis-like' single-gene disorders and familial multiple sclerosis.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 705, doi. 10.1007/s00439-017-1784-9
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- Publication type:
- Article
Rare SLC1A1 variants in hot water epilepsy.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 693, doi. 10.1007/s00439-017-1778-7
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- Publication type:
- Article
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 665, doi. 10.1007/s00439-017-1779-6
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- Article
Erratum to: Complete mitochondrial genomes of Thai and Lao populations indicate an ancient origin of Austroasiatic groups and demic diffusion in the spread of Tai-Kadai languages.
- Published in:
- 2017
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- Publication type:
- Erratum
Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 715, doi. 10.1007/s00439-017-1782-y
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- Publication type:
- Article
Sequential recruitment of study participants may inflate genetic heritability estimates.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 743, doi. 10.1007/s00439-017-1785-8
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- Publication type:
- Article
A genome-wide study of Hardy-Weinberg equilibrium with next generation sequence data.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 727, doi. 10.1007/s00439-017-1786-7
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- Publication type:
- Article
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 771, doi. 10.1007/s00439-017-1787-6
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- Publication type:
- Article
Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 759, doi. 10.1007/s00439-017-1794-7
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- Publication type:
- Article
M.T. Dorak: Genetic association studies: background, conduct, analysis, interpretation.
- Published in:
- 2017
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- Publication type:
- Book Review
Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 679, doi. 10.1007/s00439-017-1774-y
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- Publication type:
- Article