Found: 10
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Novel parent-of-origin-specific differentially methylated loci on chromosome 16.
- Published in:
- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0655-8
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- Publication type:
- Article
Host Transcriptional Response to Influenza and Other Acute Respiratory Viral Infections – A Prospective Cohort Study.
- Published in:
- PLoS Pathogens, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.ppat.1004869
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- Publication type:
- Article
MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 21, p. 4339, doi. 10.1093/hmg/ddt283
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- Publication type:
- Article
Histone proteoform analysis reveals epigenetic changes in adult mouse brown adipose tissue in response to cold stress.
- Published in:
- Epigenetics & Chromatin, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s13072-024-00536-8
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- Publication type:
- Article
Direct and indirect nigrofugal projections to the nucleus reticularis pontis caudalis mediate in the motor execution of the acoustic startle reflex.
- Published in:
- Brain Structure & Function, 2018, v. 223, n. 6, p. 2733, doi. 10.1007/s00429-018-1654-9
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- Publication type:
- Article
Low Levels of Genetic Divergence across Geographically and Linguistically Diverse Populations from India.
- Published in:
- PLoS Genetics, 2006, v. 3, n. 6, p. 2052, doi. 10.1371/journal.pgen.0020215
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- Publication type:
- Article
Vertical transmission of a large calvarial ossification defect due to heterozygous variants of ALX4 and TWIST1.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 3, p. 916, doi. 10.1002/ajmg.a.62036
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- Publication type:
- Article
Wolff–Parkinson–White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 6, p. 1387, doi. 10.1002/ajmg.a.61571
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- Publication type:
- Article
Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 8, p. 2176, doi. 10.1002/ajmg.a.38309
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- Publication type:
- Article
Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing.
- Published in:
- 2021
- By:
- Publication type:
- journal article