Found: 11
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Evolutionary Dynamics of Human Retroviruses Investigated Through Full-Genome Scanning.
- Published in:
- Molecular Biology & Evolution, 2005, v. 22, n. 4, p. 942, doi. 10.1093/molbev/msi078
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- Publication type:
- Article
Frequent HTLV-1 infection in the offspring of Peruvian women with HTLV-1--associated myelopathy/tropical spastic paraparesis or strongyloidiasis.
- Published in:
- Pan American Journal of Public Health / Revista Panamericana de Salud Pública, 2007, v. 22, n. 4, p. 223, doi. 10.1590/S1020-49892007000900001
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- Publication type:
- Article
Patient-reported outcome measures on mental health and psychosocial factors in patients with Brugada syndrome.
- Published in:
- EP: Europace, 2023, v. 25, n. 9, p. 1, doi. 10.1093/europace/euad205
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- Publication type:
- Article
Heart rate variability and microvolt T wave alternans changes during ajmaline test may predict prognosis in Brugada syndrome.
- Published in:
- Clinical Autonomic Research, 2023, v. 33, n. 1, p. 51, doi. 10.1007/s10286-023-00922-4
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- Publication type:
- Article
Comprehensive evaluation of the implementation of episignatures for diagnosis of neurodevelopmental disorders (NDDs).
- Published in:
- Human Genetics, 2023, v. 142, n. 12, p. 1721, doi. 10.1007/s00439-023-02609-2
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- Publication type:
- Article
Understanding mutational effects in digenic diseases.
- Published in:
- Nucleic Acids Research, 2017, v. 45, n. 15, p. 1, doi. 10.1093/nar/gkx557
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- Publication type:
- Article
DIDA: A curated and annotated digenic diseases database.
- Published in:
- Nucleic Acids Research, 2016, v. 44, p. D900, doi. 10.1093/nar/gkv1068
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- Publication type:
- Article
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families.
- Published in:
- 2019
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- Publication type:
- journal article
Change in hepatitis C virus genotype in hemodialysis patients after end-of-treatment response to interferon monotherapy-relapse or re-infection?
- Published in:
- Journal of Medical Virology, 2008, v. 80, n. 1, p. 80, doi. 10.1002/jmv.21050
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- Publication type:
- Article
Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 10, p. 1, doi. 10.1002/mgg3.1776
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- Publication type:
- Article
Identification of differentially methylated regions in rare diseases from a single-patient perspective.
- Published in:
- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01403-7
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- Publication type:
- Article