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

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.

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Item Type: Journal article
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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