Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells
Open Access
- 10 June 2009
- journal article
- research article
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 17 (12), 1625-1634
- https://doi.org/10.1038/ejhg.2009.77
Abstract
No abstract availableThis publication has 42 references indexed in Scilit:
- Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndromeEuropean Journal of Human Genetics, 2008
- Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysisEuropean Journal of Human Genetics, 2008
- Twin-Specific Intrauterine ‘Growth’ Charts Based on Cross-Sectional Birthweight DataTwin Research and Human Genetics, 2008
- The epigenetic imprinting defect of patients with Beckwith--Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 regionJournal of Medical Genetics, 2006
- New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeCytogenetic and Genome Research, 2006
- Epimutation of the TNDM locus and the Beckwith–Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitusHuman Genetics, 2006
- Monozygotic twins with discordant karyotypes: a case reportThe Journal of Pediatrics, 2004
- Imprinting Status of 11p15 Genes in Beckwith–Wiedemann Syndrome Patients with CDKN1C MutationsGenomics, 2001
- Twins and twinningAmerican Journal of Medical Genetics, 1996
- Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potentialThe Journal of Pediatrics, 1980