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Genomic sister-disorders of neurodevelopment: an evolutionary approach
Genomic sister-disorders are defined here as diseases mediated by duplications versus deletions of the same region. Such disorders can provide unique information concerning the genomic underpinnings of human neurodevelopment because effects of diametric variation in gene copy number on cognitive and...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Blackwell Publishing Ltd
2009
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352408/ https://www.ncbi.nlm.nih.gov/pubmed/25567849 http://dx.doi.org/10.1111/j.1752-4571.2008.00056.x |