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

Bengesser, K., Cooper, D.N., Steinmann, K., Kluwe, L., Chuzhanova, N.A. ORCID: 0000-0002-4655-3618, Wimmer, K., Tinschert, S., Mautner, V. and Kehrer-Sawatzki, H., 2010. A novel third type of recurrent NF1 microdeletion mediated by non-allelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2. Human Mutation, 31, pp. 742-751.

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Item Type: Journal article
Publication Title: Human Mutation
Creators: Bengesser, K., Cooper, D.N., Steinmann, K., Kluwe, L., Chuzhanova, N.A., Wimmer, K., Tinschert, S., Mautner, V. and Kehrer-Sawatzki, H.
Date: 2010
Volume: 31
Divisions: Schools > School of Science and Technology
Depositing User: EPrints Services
Date Added: 09 Oct 2015 10:22
Last Modified: 09 Jun 2017 13:27
URI: http://irep.ntu.ac.uk/id/eprint/11817

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