Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith–Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region
Tatsuki Urakawa(National Center For Child Health and Development), Masayo Kagami(National Center For Child Health and Development), Naoko Amano(Saitama Municipal Hospital), Yuri Kanamaru(National Center For Child Health and Development), Maki Fukami(National Center For Child Health and Development), Akira Uchida(Hiroshima City Asa Citizens Hospital)
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