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1 research outputs found
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1
Author
Docherty LE
Gicquel C
+6Â more
Leith DJ
Mackay DJG
Poole RL
Shmela ME
Splitt M
Temple K
Publication venue
Nature Publishing Group
Publication date
24/08/2011
Field of study
No full text
Newcastle University E-Prints