Works:
- Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes
- Einzellokus- und Multilokus-Methylierungsstörungen beim Silver-Russell-Syndrom : Häufigkeiten und funktionelle Relevanz
- Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
- Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation