Chuzhanova, N. ORCID: 0000-0002-4655-3618, Abeysinghe, S.S., Krawczak, M. and Cooper, D.N., 2003. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends. Human Mutation, 22 (3), pp. 245-251.
Full text not available from this repository.Item Type: | Journal article |
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Publication Title: | Human Mutation |
Creators: | Chuzhanova, N., Abeysinghe, S.S., Krawczak, M. and Cooper, D.N. |
Date: | 2003 |
Volume: | 22 |
Number: | 3 |
Divisions: | Schools > School of Science and Technology |
Record created by: | EPrints Services |
Date Added: | 09 Oct 2015 11:02 |
Last Modified: | 09 Jun 2017 13:47 |
URI: | https://irep.ntu.ac.uk/id/eprint/21765 |
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