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, DN, Steinmann, K, Kluwe, L, Chuzhanova, NA ORCID logoORCID: https://orcid.org/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.

Full text not available from this repository.
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
Record created by: EPrints Services
Date Added: 09 Oct 2015 10:22
Last Modified: 09 Jun 2017 13:27
URI: https://irep.ntu.ac.uk/id/eprint/11817

Actions (login required)

Edit View Edit View

Statistics

Views

Views per month over past year

Downloads

Downloads per month over past year