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: https://orcid.org/0000-0002-4655-3618, Abeysinghe, SS, Krawczak, M and Cooper, DN, 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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