Found: 19
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Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy.
- Published in:
- Journal of Child Neurology, 2019, v. 34, n. 8, p. 472, doi. 10.1177/0883073819840449
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- Publication type:
- Article
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
- Published in:
- BMC Genomics, 2015, v. 16, p. S12, doi. 10.1186/1471-2164-16-S1-S12
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- Publication type:
- Article
Structural variants: changing the landscape of chromosomes and design of disease studies.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. suppl_1, p. R57, doi. 10.1093/hmg/ddl057
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- Publication type:
- Article
Structural variants: changing the landscape of chromosomes and design of disease studies.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 1, p. r57, doi. 10.1093/hmg/ddl057
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- Publication type:
- Article
Clinically relevant copy number variations detected in cerebral palsy.
- Published in:
- Nature Communications, 2015, v. 6, n. 8, p. 7949, doi. 10.1038/ncomms8949
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- Publication type:
- Article
Erratum: A genotype resource for postmortem brain samples from the Autism Tissue Program.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2011, v. 4, n. 4, p. 314, doi. 10.1002/aur.211
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- Publication type:
- Article
A genotype resource for postmortem brain samples from the Autism Tissue Program.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2011, v. 4, n. 2, p. 89, doi. 10.1002/aur.173
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- Publication type:
- Article
Chromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomics.
- Published in:
- G3: Genes | Genomes | Genetics, 2022, v. 12, n. 8, p. 1, doi. 10.1093/g3journal/jkac138
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- Publication type:
- Article
Mutational Landscape of Autism Spectrum Disorder Brain Tissue.
- Published in:
- Genes, 2022, v. 13, n. 2, p. 207, doi. 10.3390/genes13020207
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- Publication type:
- Article
Functional variants of OCTN cation transporter genes are associated with Crohn disease.
- Published in:
- Nature Genetics, 2004, v. 36, n. 5, p. 471, doi. 10.1038/ng1339
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- Publication type:
- Article
A Distributed Whole Genome Sequencing Benchmark Study.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.612515
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- Publication type:
- Article
VikNGS: a C++ variant integration kit for next generation sequencing association analysis.
- Published in:
- Bioinformatics, 2020, v. 36, n. 4, p. 1283, doi. 10.1093/bioinformatics/btz716
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- Publication type:
- Article
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes.
- Published in:
- Biomolecules (2218-273X), 2024, v. 14, n. 5, p. 569, doi. 10.3390/biom14050569
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- Publication type:
- Article
Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans.
- Published in:
- EMBO Journal, 2004, v. 23, n. 2, p. 473, doi. 10.1038/sj.emboj.7600057
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- Publication type:
- Article
Copy number variation in fetal alcohol spectrum disorder.
- Published in:
- Biochemistry & Cell Biology, 2018, v. 96, n. 2, p. 161, doi. 10.1139/bcb-2017-0241
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- Publication type:
- Article
DLG5 variants contribute to Crohn disease risk in a Canadian population.
- Published in:
- Human Mutation, 2006, v. 27, n. 4, p. 353, doi. 10.1002/humu.20301
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- Publication type:
- Article
Cerebral palsy and genomics: an international consortium.
- Published in:
- 2018
- By:
- Publication type:
- letter
Gene copy number variation and pediatric mental health/neurodevelopment in a general population.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 15, p. 2411, doi. 10.1093/hmg/ddad074
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- Publication type:
- Article
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.
- Published in:
- 2018
- By:
- Publication type:
- journal article