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Is it Williams Syndrome? GTF2IRD1 implicated in Visual-Spatial Construction and GTF2I in Sociability Revealed by High Resolution Arrays
Genetic contributions to human cognition and behavior are clear but difficult to define. Williams syndrome (WS) provides a unique model for relating single genes to visual-spatial cognition and social behavior. We defined a ~1.5 Mb region of ~25 genes deleted in >98% of typical WS and then rare s...
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| Autores principales: | , , , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2009
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2650741/ https://ncbi.nlm.nih.gov/pubmed/19205026 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.32652 |
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