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Q54401181-6C5149A5-F2BF-4F5C-BD23-D46A69452AC4
Q54401181-6C5149A5-F2BF-4F5C-BD23-D46A69452AC4
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http://www.wikidata.org/entity/statement/Q54401181-6C5149A5-F2BF-4F5C-BD23-D46A69452AC4
High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.
P2860
Q54401181-6C5149A5-F2BF-4F5C-BD23-D46A69452AC4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54401181-6C5149A5-F2BF-4F5C-BD23-D46A69452AC4
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wasDerivedFrom
f63ee1856fcf114bddeb50445a258e180215891f
P2860
Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.