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Items: 1 to 20 of 206

1.

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.

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.

[Genetics of specific language impairments].

Bonneau D, Verny C, Uzé J.

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

PMID:
15475279
4.

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.

5.

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
6.

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

MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE.

Am J Hum Genet. 2005 Jun;76(6):1074-80. Epub 2005 Apr 22.

7.

Molecular genetics of speech and language disorders.

Newbury DF, Monaco AP.

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

PMID:
12436038
8.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
9.

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
10.

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
11.

A grammatical specific language impairment in children: an autosomal dominant inheritance?

van der Lely HK, Stollwerck L.

Brain Lang. 1996 Mar;52(3):484-504.

PMID:
8653392
12.

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
13.
14.

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
15.

A major susceptibility locus for specific language impairment is located on 13q21.

Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM.

Am J Hum Genet. 2002 Jul;71(1):45-55. Epub 2002 Jun 4.

16.

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.

17.

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
18.

Evaluation of FOXP2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, Sheffield VC.

Am J Med Genet. 2002 Jul 8;114(5):566-9.

PMID:
12116195
19.

Specific language impairment in families: evidence for co-occurrence with reading impairments.

Flax JF, Realpe-Bonilla T, Hirsch LS, Brzustowicz LM, Bartlett CW, Tallal P.

J Speech Lang Hear Res. 2003 Jun;46(3):530-43.

PMID:
14696984
20.

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

Tolosa A, Sanjuán J, Dagnall AM, Moltó MD, Herrero N, de Frutos R.

BMC Med Genet. 2010 Jul 22;11:114. doi: 10.1186/1471-2350-11-114.

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