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ejhg.2011.166
ejhg.2011.166
https://scigraph.springernature.com/pub.10.1038/ejhg.2011.166
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.
P2888
Q40492792-F33A2193-463B-4F31-8DA7-D04757B02250
P2888
ejhg.2011.166
https://scigraph.springernature.com/pub.10.1038/ejhg.2011.166