A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

Autor: Georgina Kearsley, Helen Cockerill, Catherine Wainhouse, Tom Berney, Anne Schönewald, Ros Packer, Catherine Lord, Rodney M. J. Cotterill, Demetrious Haracopos, Anne Gilchrist, Edwin H. Cook, Michael G. Daker, Sabine M. Klauck, Anne Aubin, Ann Le Couteur, Patrick Bolton, Jane Whittaker, Eric Fombonne, Sven Bölte, Janine A. Lamb, Chantal Kemner, Angela J. Marlow, Pat Scudder, Gabriele Schmötzer, Nicola Matthews, Evelyne Arti-Vartayan, Elena Maestrini, Michael Rutter, Katerina Papanikolaou, Gillian Baird, Annemarie Poustka, Ami Klin, Anja Spieler, Fritz Poustka, Amaia Hervas, Daniel E. Weeks, Simon Wallace, Anthony Cox, Jonathan Green, Susan L. Smalley, Sarah Palferman, Maretha de Jonge, Clyde Francks, Fleming Nuffield, Zandra Deans, Lennart Pederson, Anthony J. Bailey, Fred Volkmar, Bryan Bolton, Dorothea Rühl, Bernadette Rogé, Anthony P. Monaco, Janine Michelotti, Karen Brøndum-Nielsen, Jeanne Fremolle-Kruck, Zoe Docherty, Ineke Den Hartog, Bennett L. Leventhal, David Pauls, Herman van Engeland, Caroline Mackie Ogilvie, Maïté Tauber, Thomas Kelly, Hayley Cooper

Publikováno v: Human Molecular Genetics

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 str

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