The two-domain hypothesis in Beckwith-Wiedemann syndrome
- 15 September 2000
- journal article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 106 (6), 739-740
- https://doi.org/10.1172/jci10911
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Beckwith-Wiedemann syndrome: imprinting in clusters revisitedJournal of Clinical Investigation, 2000
- LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybridsHuman Molecular Genetics, 1999
- Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationJournal of Medical Genetics, 1999
- Loss of imprinting of a paternally expressed transcript, with antisense orientation to K V LQT1, occurs frequently in Beckwith–Wiedemann syndrome and is independent of insulin-like growth factor II imprintingProceedings of the National Academy of Sciences, 1999
- Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.1998
- Relaxation of imprinted genes in human cancerNature, 1993