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

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.

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Item Type: Journal article
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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