Figure 1From: Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjectsFrequencies of Beckwith-Wiedemann syndrome clinical features according to molecular subtype. (a) Hemihypertrophy, (b) macroglossia, (c) facial naevus flammeus, (d) ear creases/pits, (e) exomphalos, (f) organomegaly, and (g) embryonal tumours. ALL-MUT, all mutations; IC1, imprinting centre 1; IC2, imprinting centre 2; NIL, no mutations; pUPD, paternal uniparental disomy.Back to article page