A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
Autism is characterized by impairments in reciprocal social interaction and communication, and restricted and sterotyped patterns of interests and activities. Developmental difficulties are apparent before 3 years of age and there is evidence for strong genetic influences most likely involving more...
المؤلفون الرئيسيون: | Bailey, A, Hervas, A, Matthews, N, Palferman, S, Wallace, S, Aubin, A, Michelotti, J, Wainhouse, C, Papanikolaou, K, Rutter, M, Maestrini, E, Marlow, A, Weeks, D, Lamb, J, Francks, C, Kearsley, G, Scudder, P, Monaco, A, Baird, G, Cox, A, Cockerill, H, Le Couteur, A, Berney, T, Cooper, H, Kelly, T |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1998
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مواد مشابهة
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Molecular genetic investigations of autism.
حسب: Maestrini, E, وآخرون
منشور في: (1998) -
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.
حسب: Maestrini, E, وآخرون
منشور في: (1999) -
International molecular genetic study of autism consortium (IMGSAC). Towards identification of autism susceptibility variants in the IMGSAC sample
حسب: Lamb, J, وآخرون
منشور في: (2004) -
Identifying autism susceptibility genes.
حسب: Maestrini, E, وآخرون
منشور في: (2000) -
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p: International molecular genetic study of autism consortium, (IMGSAC)
حسب: Monaco, A
منشور في: (2001)