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Items: 1 to 20 of 66

1.

An Investigation of Language Impairment in Autism: Implications for Genetic Subgroups.

Kjelgaard MM, Tager-Flusberg H.

Lang Cogn Process. 2001 Apr 1;16(2-3):287-308.

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Abnormal asymmetry in language association cortex in autism.

Herbert MR, Harris GJ, Adrien KT, Ziegler DA, Makris N, Kennedy DN, Lange NT, Chabris CF, Bakardjiev A, Hodgson J, Takeoka M, Tager-Flusberg H, Caviness VS Jr.

Ann Neurol. 2002 Nov;52(5):588-96.

PMID:
12402256
5.

Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives.

Dawson G, Webb S, Schellenberg GD, Dager S, Friedman S, Aylward E, Richards T.

Dev Psychopathol. 2002 Summer;14(3):581-611. Review.

PMID:
12349875
6.

Cognitive profiles and social-communicative functioning in children with autism spectrum disorder.

Joseph RM, Tager-Flusberg H, Lord C.

J Child Psychol Psychiatry. 2002 Sep;43(6):807-21.

7.

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
8.

Language-impaired children: No sign of the FOXP2 mutation.

Meaburn E, Dale PS, Craig IW, Plomin R.

Neuroreport. 2002 Jun 12;13(8):1075-7.

PMID:
12060812
9.

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.

10.

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.

11.

Genetics of autism: complex aetiology for a heterogeneous disorder.

Folstein SE, Rosen-Sheidley B.

Nat Rev Genet. 2001 Dec;2(12):943-55. Review.

PMID:
11733747
12.

Talk of genetics and vice versa.

Pinker S.

Nature. 2001 Oct 4;413(6855):465-6. No abstract available.

PMID:
11586336
13.

Annotation: the cognitive neuroscience of face recognition: implications for developmental disorders.

Elgar K, Campbell R.

J Child Psychol Psychiatry. 2001 Sep;42(6):705-17. Review.

PMID:
11583243
14.

Nonword repetition performance in school-age children with and without language impairment.

Ellis Weismer S, Tomblin JB, Zhang X, Buckwalter P, Chynoweth JG, Jones M.

J Speech Lang Hear Res. 2000 Aug;43(4):865-78.

PMID:
11386474
15.

Macrocephaly in autism and other pervasive developmental disorders.

Fidler DJ, Bailey JN, Smalley SL.

Dev Med Child Neurol. 2000 Nov;42(11):737-40.

16.

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.

Lord C, Risi S, Lambrecht L, Cook EH Jr, Leventhal BL, DiLavore PC, Pickles A, Rutter M.

J Autism Dev Disord. 2000 Jun;30(3):205-23.

PMID:
11055457
17.

Genetic studies of autism: from the 1970s into the millennium.

Rutter M.

J Abnorm Child Psychol. 2000 Feb;28(1):3-14. Review.

PMID:
10772346
18.

Autism: recent molecular genetic advances.

Lamb JA, Moore J, Bailey A, Monaco AP.

Hum Mol Genet. 2000 Apr 12;9(6):861-8. Review. Erratum in: Hum Mol Genet 2000 May 22;9(9):1461.

19.

Value of a clinical morphology examination in autism.

Miles JH, Hillman RE.

Am J Med Genet. 2000 Apr 10;91(4):245-53.

PMID:
10766977
20.

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY.

Nat Genet. 1999 Oct;23(2):185-8.

PMID:
10508514
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