The Origin ofEFNB1Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males


Stephen R.F. Twigg,Kazuya Matsumoto,Alexa M.J. Kidd,Anne Goriely,Indira B. Taylor,Richard B. Fisher,A. Jeannette M. Hoogeboom,Irene M.J. Mathijssen,M. Teresa Lourenço,Jenny E.V. Morton,Elizabeth Sweeney,Louise C. Wilson,Han G. Brunner, et al.


The American Journal of Human Genetics




June 2006

Copyright © 2006, Elsevier

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