Evidence for Linkage and Association with Reading Disability, on 6p21.3-22

Reading disability (RD), or dyslexia, is a common heterogeneous syndrome with a large genetic component. Several studies have consistently found evidence for a quantitative-trait locus (QTL) within the 17 Mb (14.9 cM) that span D6S109 and D6S291 on chromosome 6p21.3-22. To characterize further linka...

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Main Authors: Kaplan, D. E., Gayán, J., Ahn, J., Won, T.-W., Pauls, D., Olson, R. K., DeFries, J. C., Wood, F., Pennington, B. F., Page, G. P., Smith, S. D., Gruen, J. R.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2002
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC447603/
https://ncbi.nlm.nih.gov/pubmed/11951179
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