Identification of differentially methylated regions in rare diseases from a single-patient perspective
Article in Clinical Epigenetics (December 2022)
The most recent citing publications are shown below. View all 5 publications that cite this research output on Dimensions.
Beckwith-Wiedemann syndrome with long QT caused by a deletion involving KCNQ1 but not KCNQ1OT1:TSS-DMR
Article in European Journal of Medical Genetics (November 2022)
Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome
Article in Expert Review of Endocrinology & Metabolism (November 2022)