Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 230

1.

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
2.

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW.

Am J Med Genet A. 2006 Mar 1;140(5):509-14.

PMID:
16470794
3.

Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment.

Palka C, Alfonsi M, Mohn A, Cerbo R, Guanciali Franchi P, Fantasia D, Morizio E, Stuppia L, Calabrese G, Zori R, Chiarelli F, Palka G.

Pediatrics. 2012 Jan;129(1):e183-8. doi: 10.1542/peds.2010-2094. Epub 2011 Dec 5.

PMID:
22144704
4.

A forkhead-domain gene is mutated in a severe speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP.

Nature. 2001 Oct 4;413(6855):519-23.

PMID:
11586359
5.

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP.

Am J Hum Genet. 2000 Aug;67(2):357-68. Epub 2000 Jul 5.

6.

Localisation of a gene implicated in a severe speech and language disorder.

Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME.

Nat Genet. 1998 Feb;18(2):168-70. Erratum in: Nat Genet 1998 Mar;18(3):298.

PMID:
9462748
7.

De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment.

Kosho T, Sakazume S, Kawame H, Wakui K, Wada T, Okoshi Y, Mikawa M, Hasegawa T, Matsuura N, Niikawa N, Matsumoto N, Fukushima Y.

Clin Dysmorphol. 2008 Jan;17(1):31-4.

PMID:
18049078
8.

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.

Warburton P, Baird G, Chen W, Morris K, Jacobs BW, Hodgson S, Docherty Z.

Am J Med Genet. 2000 Apr 3;96(2):228-34.

PMID:
10893502
9.

The WNT2 gene polymorphism associated with speech delay inherent to autism.

Lin PI, Chien YL, Wu YY, Chen CH, Gau SS, Huang YS, Liu SK, Tsai WC, Chiu YN.

Res Dev Disabil. 2012 Sep-Oct;33(5):1533-40. doi: 10.1016/j.ridd.2012.03.004. Epub 2012 Apr 21.

PMID:
22522212
10.

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.

Manning MA, Cassidy SB, Clericuzio C, Cherry AM, Schwartz S, Hudgins L, Enns GM, Hoyme HE.

Pediatrics. 2004 Aug;114(2):451-7.

PMID:
15286229
11.

FOXP2 is not a major susceptibility gene for autism or specific language impairment.

Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium.

Am J Hum Genet. 2002 May;70(5):1318-27. Epub 2002 Mar 13.

12.

Molecular genetics of speech and language disorders.

Newbury DF, Monaco AP.

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

PMID:
12436038
13.

Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.

Li H, Yamagata T, Mori M, Momoi MY.

Brain Dev. 2005 Apr;27(3):207-10.

PMID:
15737702
14.

Association of specific language impairment (SLI) to the region of 7q31.

O'Brien EK, Zhang X, Nishimura C, Tomblin JB, Murray JC.

Am J Hum Genet. 2003 Jun;72(6):1536-43. Epub 2003 Apr 29.

15.

Phenotype of FOXP2 haploinsufficiency in a mother and son.

Rice GM, Raca G, Jakielski KJ, Laffin JJ, Iyama-Kurtycz CM, Hartley SL, Sprague RE, Heintzelman AT, Shriberg LD.

Am J Med Genet A. 2012 Jan;158A(1):174-81. doi: 10.1002/ajmg.a.34354. Epub 2011 Nov 21.

16.

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.

Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K.

Am J Hum Genet. 2006 Nov;79(5):965-72. Epub 2006 Sep 27.

17.

Association between the FOXP2 gene and autistic disorder in Chinese population.

Gong X, Jia M, Ruan Y, Shuang M, Liu J, Wu S, Guo Y, Yang J, Ling Y, Yang X, Zhang D.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):113-6.

PMID:
15108192
18.

Communication genes clustered on 7q31.

Ramsay M.

Mol Med Today. 2000 Oct;6(10):380-1. No abstract available.

PMID:
11006523
19.

[Genetics of specific language impairments].

Bonneau D, Verny C, Uzé J.

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

PMID:
15475279
20.

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

Supplemental Content

Support Center