Imprinting defects on human chromosome 15
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics,Molecular Biology
Reference56 articles.
1. De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
2. Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L
3. Bourc'his D, Xu GL, Lin CS, Bollman B, Bestor TH: Dnmt3L and the establishment of maternal genomic imprints. Science294:2536-2539 (2001).
4. The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
5. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15
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