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Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in
J Swensen1, C M Lewis, L A Cannon-Albright
1Department of Medical Informatics, University of Utah, Salt Lake City 84108, USA.
Human Mutation
|January 1, 1997
Abstract
No abstract available in PubMed .
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