Endophenotypes of FOXP2: dysfunction within the human articulatory network
F Liégeois, AT Morgan, A Connelly… - European Journal of …, 2011 - Elsevier
The identification of the first gene involved in a speech-language disorder was made
possible through the study of a British multi-generational family (the “KE family”) in whom …
possible through the study of a British multi-generational family (the “KE family”) in whom …
[PDF][PDF] Endophenotypes of FOXP2: Dysfunction within the human articulatory network
F Liegeois, AT Morgan, A Connelly… - european journal of …, 2011 - academia.edu
Investigations of a multi-generational British family (“KE” family1) in whom half the members
are affected by a speechlanguage disorder caused by a heterozygous mutation have led to …
are affected by a speechlanguage disorder caused by a heterozygous mutation have led to …
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
F Liégeois, AT Morgan, A Connelly… - European Journal of …, 2011 - europepmc.org
The identification of the first gene involved in a speech-language disorder was made
possible through the study of a British multi-generational family (the" KE family") in whom …
possible through the study of a British multi-generational family (the" KE family") in whom …
Endophenotypes of FOXP2: dysfunction within the human articulatory network
F Liégeois, AT Morgan, A Connelly… - … : official journal of …, 2011 - pubmed.ncbi.nlm.nih.gov
The identification of the first gene involved in a speech-language disorder was made
possible through the study of a British multi-generational family (the" KE family") in whom …
possible through the study of a British multi-generational family (the" KE family") in whom …
Endophenotypes of FOXP2: Dysfunction within the human articulatory network
F Liégeois, AT Morgan, A Connelly… - European Journal of …, 2011 - infona.pl
The identification of the first gene involved in a speech-language disorder was made
possible through the study of a British multi-generational family (the “KE family”) in whom …
possible through the study of a British multi-generational family (the “KE family”) in whom …
Endophenotypes of FOXP2: Dysfunction within the human articulatory network
F Liégeois, AT Morgan, A Connelly… - European Journal of …, 2011 - ejpn-journal.com
The identification of the first gene involved in a speech-language disorder was made
possible through the study of a British multi-generational family (the" KE family") in whom …
possible through the study of a British multi-generational family (the" KE family") in whom …