Use of High-Throughput Targeted Exome-Sequencing to Screen for Copy Number Variation in Hypertrophic Cardiomyopathy

AuthID
P-00J-XVP
7
Author(s)
Murphy, C
·
Syrris, P
·
Dalageorgou, C
·
McKenna, WJ
·
Plagnol, V
Document Type
Article
Year published
2015
Published
in EUROPEAN JOURNAL OF MEDICAL GENETICS, ISSN: 1769-7212
Volume: 58, Issue: 11, Pages: 611-616 (6)
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Publication Identifiers
Scopus: 2-s2.0-84948967029
Wos: WOS:000365349200009
Source Identifiers
ISSN: 1769-7212
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