Found: 8
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Complex movement disorder in a patient with heterozygous YY1 mutation (Gabriele‐de Vries syndrome).
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 9, p. 2129, doi. 10.1002/ajmg.a.61731
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- Article
LARS2-Perrault syndrome: a new case report and literature review.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01028-8
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- Article
MCF2 is linked to a complex perisylvian syndrome and affects cortical lamination.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 1, p. 121, doi. 10.1002/acn3.50949
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- Article
Bi‐allelic loss of ERGIC1 causes relatively mild arthrogryposis.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 3, p. 329, doi. 10.1111/cge.14004
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- Article
NGS-Based S. aureus Typing and Outbreak Analysis in Clinical Microbiology Laboratories: Lessons Learned From a Swiss-Wide Proficiency Test.
- Published in:
- Frontiers in Microbiology, 2020, v. 11, p. N.PAG, doi. 10.3389/fmicb.2020.591093
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- Article
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients.
- Published in:
- Human Mutation, 2021, v. 42, n. 4, p. 373, doi. 10.1002/humu.24167
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- Article
No evidence for the radiation time lag model after whole genome duplications in Teleostei.
- Published in:
- PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0176384
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- Article
Detecting patterns of species diversification in the presence of both rate shifts and mass extinctions.
- Published in:
- BMC Evolutionary Biology, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12862-015-0432-z
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- Article