Phenotype of FOXP2 haploinsufficiency in a mother and son-Reference-Cited by-同舟云学术

Phenotype of FOXP2 haploinsufficiency in a mother and son

Published:2011-11-21 Issue:1 Volume:158A Page:174-181
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Rice Gregory M.,Raca Gordana,Jakielski Kathy J.,Laffin Jennifer J.,Iyama-Kurtycz Christina M.,Hartley Sigan L.,Sprague Rae E.,Heintzelman Anne T.,Shriberg Lawrence D.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34354/fullpdf

Reference45 articles.

1. American Speech-Language-Hearing Association 2007 Childhood apraxia of speech [Technical report] www.asha.org/policy

2. Associations of postural knowledge and basic motor skill with dyspraxia in autism: Implication for abnormalities in distributed connectivity and motor learning;Dowell;Neuropsychology,2009

3. Absence of a paternally-inherited FOXP2 gene in developmental verbal dyspraxia;Feuk;Am J Hum Genet,2006

4. The eloquent ape: Genes, brains and the evolution of language;Fisher;Nat Rev Genet,2006

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