Genetic variants within the second intron of theKCNQ1gene affect CTCF binding and confer a risk of Beckwith–Wiedemann syndrome upon maternal transmission
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Title
Genetic variants within the second intron of theKCNQ1gene affect CTCF binding and confer a risk of Beckwith–Wiedemann syndrome upon maternal transmission
Authors
Keywords
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Journal
JOURNAL OF MEDICAL GENETICS
Volume 51, Issue 8, Pages 502-511
Publisher
BMJ
Online
2014-07-05
DOI
10.1136/jmedgenet-2014-102368
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