Browsing "Paediatrics publications" by Author Bain, N.
Showing results 1 to 1 of 1
Preview | Issue Date | Title | Author(s) |
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2013 | FOXP1 mutations cause intellectual disability and a recognizable phenotype | Le Fevre, A.; Taylor, S.; Malek, N.; Horn, D.; Carr, C.; Abdul-Rahman, O.; O'Donnell, S.; Burgess, T.; Shaw, M.; Gecz, J.; Bain, N.; Fagan, K.; Hunter, M. |