A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p

  1. Lookup NU author(s)
  2. Dr Jeremy Parr
  3. Professor Ann Le Couteur
  4. Professor Helen McConachie
  5. Dr Thomas Berney
  6. Dr Thomas Kelly
Author(s)Le Couteur A; Kelly TP; Berney T; McConachie HR; Parr J; Palferman S; Matthews N; Turner M; Moore J; Hervas A; Aubin A; Wallace S; Michelotti J; Wainhouse C; Paul A; Thompson E; Gupta R; Garner C; Murin M; Freitag C; Ryder N; Cottington E; Pickles A; Rutter M; Bailey A; Barnby G; Lamb JA; Marlow A; Scudder P; Monaco AP; Baird G; Cox A; Docherty Z; Warburton P; Green EP; Abbs SJ; De Vries PJ; Bolton PF; Green J; Gilchrist A; Whittacker J; Bolton B; Packer R; Maestrini E; Blasi F; Van Engeland H; De Jonge MV; Kemner C; Klauck SM; Beyer KS; Epp S; Poustka A; Benner A; Goethe JW; Poustka F; Ruhl D; Schmotzer G; Boolte S; Feineis-Matthews S; Fombonne E; Rogee B; Fremolle-Kruck J; Pienkowski C; Tauber MT; Pedersen L; Nielsen KB; Eriksen G; Haracopos D; Cotterill RMJ; Tsiantis J; Papanikolaou K; Lord C; Corsello C; Guter S; Leventhal B; Cook E; Smalley SL; Bailey J; McGough J; Levitt J; Pauls D; Volkmar F; Weeks DE; Int Mol Genetic Study Autism Cons
Publication type Article
JournalAmerican Journal of Human Genetics
Year2001
Volume69
Issue3
Pages570-581
ISSN (print)0002-9297
ISSN (electronic)1537-6605
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
PublisherCell Press
URLhttp://dx.doi.org/10.1086/323264
DOI10.1086/323264
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