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Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID)
BACKGROUND: DNA copy number variants (CNVs) are found in 15% of subjects with ID but their association with phenotypic abnormalities has been predominantly studied in smaller cohorts of subjects with detailed yet non-systematically categorized phenotypes, or larger cohorts (thousands of cases) with...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107469/ https://www.ncbi.nlm.nih.gov/pubmed/25030379 http://dx.doi.org/10.1186/1471-2350-15-82 |