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Items: 10

1.

Mutation screening of FOXP2 in individuals diagnosed with autistic disorder.

Gauthier J, Joober R, Mottron L, Laurent S, Fuchs M, De Kimpe V, Rouleau GA.

Am J Med Genet A. 2003 Apr 15;118A(2):172-5.

PMID:
12655497
2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
3.

Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.

Lennon PA, Cooper ML, Peiffer DA, Gunderson KL, Patel A, Peters S, Cheung SW, Bacino CA.

Am J Med Genet A. 2007 Apr 15;143A(8):791-8. Review.

PMID:
17330859
4.

Molecular genetics of speech and language disorders.

Newbury DF, Monaco AP.

Curr Opin Pediatr. 2002 Dec;14(6):696-701. Review.

PMID:
12436038
6.

FOXP2 as a molecular window into speech and language.

Fisher SE, Scharff C.

Trends Genet. 2009 Apr;25(4):166-77. doi: 10.1016/j.tig.2009.03.002. Epub 2009 Mar 21. Review.

PMID:
19304338
7.

Deciphering the genetic basis of speech and language disorders.

Fisher SE, Lai CS, Monaco AP.

Annu Rev Neurosci. 2003;26:57-80. Epub 2003 Jan 8. Review.

PMID:
12524432
8.

[Genetic factors in the development of language].

Sanjuán J, Tolosa A, Colomer-Revuelta J, Ivorra-Martínez J, Llacer B, Jover M.

Rev Neurol. 2010 Mar 3;50 Suppl 3:S101-6. Review. Spanish.

9.

What can mice tell us about Foxp2 function?

French CA, Fisher SE.

Curr Opin Neurobiol. 2014 Oct;28:72-9. doi: 10.1016/j.conb.2014.07.003. Epub 2014 Jul 19. Review.

PMID:
25048596
10.

[Problematic aspects of the genetic analysis of the specific disorders of the language: FOXP2 as paradigm].

Benítez-Burraco A.

Neurologia. 2012 May;27(4):225-33. doi: 10.1016/j.nrl.2011.04.008. Epub 2011 Jun 8. Review. Spanish.

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