Vogt, J, Mussotter, T, Bengesser, K, Claes, K, Högel, J, Chuzhanova, N ORCID: https://orcid.org/0000-0002-4655-3618, Fu, C, Van den Ende, J, Mautner, VF, Cooper, DN, Messiaen, L and Kehrer-Sawatzki, H, 2012. Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder. Human Mutation, 33 (11), pp. 1599-1609.
Full text not available from this repository.Item Type: | Journal article |
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Publication Title: | Human Mutation |
Creators: | Vogt, J., Mussotter, T., Bengesser, K., Claes, K., Högel, J., Chuzhanova, N., Fu, C., Van den Ende, J., Mautner, V.F., Cooper, D.N., Messiaen, L. and Kehrer-Sawatzki, H. |
Date: | 2012 |
Volume: | 33 |
Number: | 11 |
Divisions: | Schools > School of Science and Technology |
Record created by: | EPrints Services |
Date Added: | 09 Oct 2015 10:20 |
Last Modified: | 09 Jun 2017 13:26 |
URI: | https://irep.ntu.ac.uk/id/eprint/11507 |
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