Relaxation of Insulin-like Growth Factor 2 Imprinting and Discordant Methylation at KvDMR1 in Two First Cousins Affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber Syndromes
- 1 March 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (3) , 841-847
- https://doi.org/10.1086/302811
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- The Role of Histone Acetylation in the Allelic Expression of the Imprinted Human Insulin-like Growth Factor II GeneBiochemical and Biophysical Research Communications, 1998
- Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith–Wiedemann and Simpson–Golabi–Behmel syndromesGenes & Development, 1997
- Expression and parental imprinting of the H19 gene in human rhabdomyosarcomaOncogene, 1997
- Involvement of IGF-II in human cancerJournal of Endocrinology, 1996
- Klippel‐Trenaunay‐Weber syndrome associated with a 5:11 balanced translocationAmerican Journal of Medical Genetics, 1995
- Epigenetic lesions at the H19 locus in Wilms' tumour patientsNature Genetics, 1994
- Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumourNature Genetics, 1994
- Functional Polymorphism in the Parental Imprinting of the Human IGF2R GeneBiochemical and Biophysical Research Communications, 1993
- Klippel-Trenaunay syndrome: is it a paradominant trait?British Journal of Dermatology, 1993
- Improving the polymorphism content of the 3′ UTR of the human IGF2R geneHuman Molecular Genetics, 1992