Chapter 8 Genomic Imprinting and Imprinting Defects in Humans
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Elsevier
Reference50 articles.
1. Gadd45a promotes epigenetic gene activation by repair‐mediated DNA demethylation;Barreto;Nature,2007
2. De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch;Bielinska;Nat. Genet.,2000
3. The SNRPN promoter is not required for genomic imprinting of the Prader‐Willi/Angelman domain in mice;Bressler;Nat. Genet.,2001
4. Inherited microdeletions in the Angelman and Prader‐Willi syndromes define an imprinting centre on human chromosome 15;Buiting;Nat. Genet.,1995
5. Sporadic imprinting defects in Prader‐Willi syndrome and Angelman syndrome: Implications for imprint‐switch models, genetic counseling, and prenatal diagnosis;Buiting;Am. J. Hum. Genet.,1998
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