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[HTML][HTML] Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

KD MacDermot, E Bonora, N Sykes, AM Coupe… - The American Journal of …, 2005 - cell.com
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …
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Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

KD MacDermot, E Bonora, N Sykes, AM Coupe… - The American Journal of …, 2005 - infona.pl
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …
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[HTML][HTML] Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

KD MacDermot, E Bonora, N Sykes, AM Coupe… - The American Journal of …, 2005 - Elsevier
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …
[PDF] core.ac.uk

[PDF][PDF] Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

KD MacDermot, E Bonora, N Sykes, AM Coupe… - Am. J. Hum …, 2005 - core.ac.uk
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

KD MacDermot, E Bonora, N Sykes… - American Journal of …, 2005 - pure.mpg.de
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …
[HTML] nih.gov

[HTML][HTML] Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

KD MacDermot, E Bonora, N Sykes… - American Journal of …, 2005 - ncbi.nlm.nih.gov
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

KD MacDermot, E Bonora… - American …, 2005 - research-portal.st-andrews.ac.uk
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …

[引用][C] Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

KD MacDermot, E Bonora, N Sykes… - The American Journal …, 2005 - cir.nii.ac.jp
Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language
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Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

KD Macdermot, E Bonora, N Sykes… - … JOURNAL OF HUMAN …, 2005 - cris.unibo.it
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …
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[PDF][PDF] Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

KD MacDermot, E Bonora, N Sykes, AM Coupe… - Am. J. Hum …, 2005 - Citeseer
FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …