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Title
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
Authors
Pagnamenta, A. T.; Khan, H.; Walker, S.; Gerrelli, D.; Wing, K.; Bonaglia, M. C.; Giorda, R.; Berney, T.; Mani, E.; Molteni, M.; Pinto, D.; Le Couteur, A.; Hallmayer, J.; Sutcliffe, J. S.; Szatmari, P.; Paterson, A. D.; Scherer, S. W.; Vieland, V. J.; Monaco, A. P.
Publication
Journal of Medical Genetics, 2011, Vol 48, Issue 1, p48