Language fMRI abnormalities associated with FOXP2 gene mutation
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
Language fMRI abnormalities associated with FOXP2 gene mutation.
F Liegeois, T Baldeweg, A Connelly… - Nature …, 2003 - search.ebscohost.com
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
Language fMRI abnormalities associated with FOXP2 gene mutation
F Liégeois, T Baldeweg, A Connelly… - Nature …, 2003 - pubmed.ncbi.nlm.nih.gov
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
[引用][C] Language fMRI abnormalities associated with FOXP2 gene mutation
F Liégeois, T Baldeweg, A Connelly, DG Gadian… - Nature …, 2003 - cir.nii.ac.jp
[PDF][PDF] Language fMRI abnormalities associated with FOXP2 gene mutation
F Liégeois, T Baldeweg, A Connelly… - NATURE …, 2003 - academia.edu
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
Language fMRI abnormalities associated with FOXP2 gene mutation.
F Liegeois, T Baldeweg, A Connelly, DG Gadian… - Nature …, 2003 - go.gale.com
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
Language fMRI abnormalities associated with FOXP2 gene mutation.
F Liégeois, T Baldeweg, A Connelly… - Nature …, 2003 - europepmc.org
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
[PDF][PDF] Language fMRI abnormalities associated with FOXP2 gene mutation
F Liégeois, T Baldeweg, A Connelly… - NATURE …, 2003 - researchgate.net
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2 gene. We examined functional brain abnormalities associated with …
Language fMRI abnormalities associated with FOXP2 gene mutation.
F Liégeois, T Baldeweg, A Connelly… - Nature …, 2003 - psycnet.apa.org
Half the members of the KE family suffer from a speech and language disorder caused by a
mutation in the FOXP2gene. We examined functional brain abnormalities associated with …
mutation in the FOXP2gene. We examined functional brain abnormalities associated with …
[引用][C] Language fMRI abnormalities associated with FOXP2 gene mutation
F LIEGEOIS - Nature Neuroscience, 2003 - cir.nii.ac.jp