Steinmann, K., Cooper, D.N., Kluwe, L., Chuzhanova, N.A. ORCID: 0000-0002-4655-3618, Senger, C., Serra, E., Lazaro, C., Wimmer, K., Mautner, V. and Kehrer-Sawatzki, H., 2007. Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination. American Journal of Human Genetics, 81, pp. 1201-1220.
Full text not available from this repository.Item Type: | Journal article |
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Publication Title: | American Journal of Human Genetics |
Creators: | Steinmann, K., Cooper, D.N., Kluwe, L., Chuzhanova, N.A., Senger, C., Serra, E., Lazaro, C., Wimmer, K., Mautner, V. and Kehrer-Sawatzki, H. |
Date: | 2007 |
Volume: | 81 |
Divisions: | Schools > School of Science and Technology |
Record created by: | EPrints Services |
Date Added: | 09 Oct 2015 10:33 |
Last Modified: | 09 Jun 2017 13:33 |
URI: | https://irep.ntu.ac.uk/id/eprint/14801 |
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