A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B‐containing low‐copy repeats in 17q11.2

K. Bengesser,D. Cooper,Katharina Steinmann,L. Kluwe,N. Chuzhanova,K. Wimmer,M. Tatagiba,S. Tinschert,V. Mautner,H. Kehrer-Sawatzki

Published 2010 in Human Mutation

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