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Q38542163-457423A8-EB8B-43D1-A081-9950CFBCBD28
Q38542163-457423A8-EB8B-43D1-A081-9950CFBCBD28
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38542163-457423A8-EB8B-43D1-A081-9950CFBCBD28
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine.
P2860
Q38542163-457423A8-EB8B-43D1-A081-9950CFBCBD28
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38542163-457423A8-EB8B-43D1-A081-9950CFBCBD28
rank
NormalRank
type
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Statement
wasDerivedFrom
7393f6e3639d963f5ee52e7046e8571ef60dbcef
P2860
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.