Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait

Multiple inquiries into the genetic etiology of human traits indicated an overlap between genes underlying monogenic disorders (eg, skeletal growth defects) and those affecting continuous variability of related quantitative traits (eg, height). Extending the idea of a shared genetic basis between a...

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Publié dans:Eur J Hum Genet
Auteurs principaux: Franić, Sanja, Groen-Blokhuis, Maria M, Dolan, Conor V, Kattenberg, Mathijs V, Pool, René, Xiao, Xiangjun, Scheet, Paul A, Ehli, Erik A, Davies, Gareth E, van der Sluis, Sophie, Abdellaoui, Abdel, Hansell, Narelle K, Martin, Nicholas G, Hudziak, James J, van Beijsterveldt, Catherina E M, Swagerman, Suzanne C, Hulshoff Pol, Hilleke E, de Geus, Eco J C, Bartels, Meike, Ropers, H Hilger, Hottenga, Jouke-Jan, Boomsma, Dorret I
Format: Artigo
Langue:Inglês
Publié: Nature Publishing Group 2015
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4592100/
https://ncbi.nlm.nih.gov/pubmed/25712083
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.3
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