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
Copyright © 2006, Elsevier
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