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Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.
10.1186/1471-2164-13-241
000308933200001
22702538
Valsesia
A.
author
Stevenson
B.J.
author
Waterworth
D.
author
Mooser
V.
author
Vollenweider
P.
author
Waeber
G.
author
Jongeneel
C.V.
author
Beckmann
J.S.
author
Kutalik
Z.
author
Bergmann
S.
author
article
2012
Bmc Genomics
1471-2164
1471-2164
journal
13
241
241
eng
60_published
true
peer-reviewed
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
https://serval.unil.ch/notice/serval:BIB_B4A4552A9706
https://serval.unil.ch/resource/serval:BIB_B4A4552A9706.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B4A4552A97069
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