Reply to "Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor"
- 1 August 2005
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 37 (8) , 786-787
- https://doi.org/10.1038/ng0805-786
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
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- Role of CTCF Binding Sites in the Igf2/H19 Imprinting Control RegionMolecular and Cellular Biology, 2004
- Mutation of a Single CTCF Target Site within the H19 Imprinting Control Region Leads to Loss of Igf2 Imprinting and Complex Patterns of De Novo Methylation upon Maternal InheritanceMolecular and Cellular Biology, 2004
- Epigenotype-phenotype correlations in Beckwith-Wiedemann syndromeJournal of Medical Genetics, 2000
- Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2Genes & Development, 1998
- The H19 Transcript Is Associated with Polysomes and May Regulate IGF2 Expression in transJournal of Biological Chemistry, 1998
- Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumourNature Genetics, 1994
- Tumour-suppressor activity of H19 RNANature, 1993