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Q41691206-83FBEE9E-9AF6-42D5-B66E-1F3627460BD1
Q41691206-83FBEE9E-9AF6-42D5-B66E-1F3627460BD1
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Statement
http://www.wikidata.org/entity/statement/Q41691206-83FBEE9E-9AF6-42D5-B66E-1F3627460BD1
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome.
P1476
Q41691206-83FBEE9E-9AF6-42D5-B66E-1F3627460BD1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41691206-83FBEE9E-9AF6-42D5-B66E-1F3627460BD1
rank
NormalRank
type
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wasDerivedFrom
5e26e625ada3c9c63006a1eb92ae29ea6c7d1bb9
P1476
A maternal deletion upstream o
......
l Beckwith-Wiedemann syndrome.
@en