Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 5

1.

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population.

Marui T, Koishi S, Funatogawa I, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Kato C, Ishijima M, Watanabe K, Kasai K, Kato N, Sasaki T.

Neurosci Res. 2005 Sep;53(1):91-4.

PMID:
15998549
2.

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
3.

Molecular genetics of speech and language disorders.

Newbury DF, Monaco AP.

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

PMID:
12436038
4.

[Genetics of specific language impairments].

Bonneau D, Verny C, Uzé J.

Arch Pediatr. 2004 Oct;11(10):1213-6. Review. French.

PMID:
15475279
5.

The early origins of autism.

Rodier PM.

Sci Am. 2000 Feb;282(2):56-63. Review. No abstract available.

PMID:
10710787

Supplemental Content

Support Center