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EJHG.2011.166
EJHG.2011.166
http://dx.doi.org/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.
P356
Q40492792-A03E13FF-C1EA-406B-A1E9-BA075EE878DB
P356
EJHG.2011.166
http://dx.doi.org/10.1038/EJHG.2011.166