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Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-99496-2
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- Article
Association between executive functions and COMT Val<sup>108/158</sup>Met polymorphism among healthy younger and older adults: A preliminary study.
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- PLoS ONE, 2024, v. 19, n. 5, p. 1, doi. 10.1371/journal.pone.0303343
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- Article
Altered White Matter Architecture in <i>BDNF</i> Met Carriers.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069290
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- Article
Genetic Diagnosis of Duchenne and Becker Muscular Dystrophy using Multiplex Ligation-Dependent Probe Amplification in Rwandan Patients.
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- Journal of Tropical Pediatrics, 2014, v. 60, n. 2, p. 112, doi. 10.1093/tropej/fmt090
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- Article
Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?
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- European Journal of Human Genetics, 2001, v. 9, n. 1, p. 1, doi. 10.1038/sj.ejhg.5200575
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- Article
Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy.
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- Journal of Inherited Metabolic Disease, 2015, v. 38, n. 6, p. 1147, doi. 10.1007/s10545-015-9857-1
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- Article
Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon-skipping therapy.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-82725-z
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- Article
Influence of COMT Genotype on Antero-posterior Cortical Functional Connectivity Underlying Interference Resolution.
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- Cerebral Cortex, 2016, v. 26, n. 2, p. 498, doi. 10.1093/cercor/bhu188
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- Article
An insertion–deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.
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- Human Molecular Genetics, 2007, v. 16, n. 24, p. 3008, doi. 10.1093/hmg/ddm259
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- Article
Concurrent Synaptic and Systems Memory Consolidation during Sleep.
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- Journal of Neuroscience, 2013, v. 33, n. 24, p. 10182, doi. 10.1523/JNEUROSCI.0284-13.2013
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- Article
Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.
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- BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-79
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- Article