Found: 8
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A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study.
- Published in:
- Frontiers in Genetics, 2016, v. 7, p. 1, doi. 10.3389/fgene.2016.00190
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- Publication type:
- Article
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2093, doi. 10.1093/hmg/ddw058
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- Publication type:
- Article
Bioassay-guided isolation of phytotoxins from three Salvia species.
- Published in:
- Allelopathy Journal, 2021, v. 54, n. 1, p. 13, doi. 10.26651/allelo.j/2021-54-1-1344
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- Publication type:
- Article
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Comprehensive Review.
- Published in:
- Diagnostics (2075-4418), 2019, v. 9, n. 3, p. 91, doi. 10.3390/diagnostics9030091
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- Publication type:
- Article
Genetic Profile of the Dystrophin Gene Reveals New Mutations in Colombian Patients Affected with Muscular Dystrophinopathy.
- Published in:
- Application of Clinical Genetics, 2021, v. 14, p. 399, doi. 10.2147/TACG.S317721
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- Publication type:
- Article
Correction: Uveitis and Multiple Sclerosis: Potential Common Causal Mutations.
- Published in:
- 2023
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- Correction Notice
Familial Alzheimer's Disease and Recessive Modifiers.
- Published in:
- Molecular Neurobiology, 2020, v. 57, n. 2, p. 1035, doi. 10.1007/s12035-019-01798-0
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- Publication type:
- Article
Uveitis and Multiple Sclerosis: Potential Common Causal Mutations.
- Published in:
- Molecular Neurobiology, 2019, v. 56, n. 12, p. 8008, doi. 10.1007/s12035-019-1630-2
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- Publication type:
- Article