Steinmann, Katharina, Cooper, David Neil ORCID: https://orcid.org/0000-0002-8943-8484, Kluwe, Lan, Chuzhanova, Nadia A., Senger, Cornelia, Serra, Eduard, Lazaro, Conxi, Gilaberte, Montserrat, Wimmer, Katharina, Mautner, Viktor-Felix and Kehrer-Sawatzki, Hildegard 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 (6) , pp. 1201-1220. 10.1086/522089 |
Official URL: http://dx.doi.org/10.1086/522089
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine |
Subjects: | R Medicine > R Medicine (General) |
Publisher: | Elsevier |
ISSN: | 0002-9297 |
Date of Acceptance: | 3 August 2007 |
Last Modified: | 31 Oct 2022 10:13 |
URI: | https://orca.cardiff.ac.uk/id/eprint/84096 |
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