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The clinical significance of small copy number variants in neurodevelopmental disorders
BACKGROUND: Despite abundant evidence for pathogenicity of large copy number variants (CNVs) in neurodevelopmental disorders (NDDs), the individual significance of genome-wide rare CNVs <500 kb has not been well elucidated in a clinical context. METHODS: By high-resolution chromosomal microarray...
Gorde:
| Egile Nagusiak: | , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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BMJ Publishing Group
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4173859/ https://ncbi.nlm.nih.gov/pubmed/25106414 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2014-102588 |
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