Genetics of childhood disorders: XLVI. Autism, part 5: Genetics of autism

Journal of the American Academy of Child and Adolescent Psychiatry

Volumn 42, Issue 1, 2003, Pages 116-118

  Veenstra Vanderweele, Jeremy ^a   Cook Jr , Edwin H ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CELL NUCLEUS DNA;

AUTISM; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; KARYOTYPING; PRIORITY JOURNAL; SHORT SURVEY; TELOMERE; CHILD; CHROMOSOME 2; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; MUTATION; REVIEW;

AUTISTIC DISORDER; CHILD; CHROMOSOMES, HUMAN, PAIR 2; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MUTATION; POLYMORPHISM, GENETIC;

EID: 0037209254     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-200301000-00018     Document Type: Article

References (9)

1. International Molecular Genetic Study of Autism Consortium (IMGSAC) A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p Am J Hum Genet 69 2001 570 581
2. Y Bradford J Haines H Hutcheson Incorporating language phenotypes strengthens evidence of linkage to autism Am J Med Genet 105 2001 539 547
3. JD Buxbaum JM Silverman CJ Smith Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity Am J Hum Genet 68 2001 1514 1520
4. JD Buxbaum JM Silverman CJ Smith Association between a GABRB3 polymorphism and autism Mol Psychiatry 7 2002 311 316
5. S Jamain C Betancur H Quach the Paris Autism Research International Sibpair (PARIS) Study Linkage and association of the glutamate receptor 6 gene with autism Mol Psychiatry 7 2002 302 310
6. SJ Kim N Cox R Courchesne Transmission disequilibrium mapping at the serotonin transporter gene ( SLC6A4 ) region in autistic disorder Mol Psychiatry 7 2002 278 288
7. CS Lai SE Fisher JA Hurst F Vargha-Khadem AP Monaco A forkhead-domain gene is mutated in a severe speech and language disorder Nature 413 2001 519 523
8. PJ Lombroso Genetics of childhood disorders, XIV: a gene for Rett syndrome: news flash J Am Acad Child Adolesc Psychiatry 39 2001 671 674
9. DF Newbury E Bonora JA Lamb the International Molecular Genetic Study of Autism Consortium FOXP2 is not a major susceptibility gene for autism or specific language impairment Am J Hum Genet 70 2002 1318 1327