Identification of Novel Exons 3′ to the HumanSNRPNGene
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference21 articles.
1. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15;Buiting;Nature Genet.,1995
2. A guanosine quadroduplex and two stable hairpins flank a major cleavage site insulin-like growth factor II mRNA;Christiansen;Nucleic Acids Res.,1994
3. Characterization of a methylation imprint in the Prader–Willi syndrome region;Dittrich;Hum. Mol. Genet.,1993
4. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene;Dittrich;Nature Genet.,1996
5. Functional imprinting and epigenetic modification of the human SNRPN gene;Glenn;Hum. Mol. Genet.,1993
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1. Prader-Willi syndrome and Angelman syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2010-08-20
2. Imprinted Genes in the Prader-Willi Deletion;Novartis Foundation Symposia;2007-09-28
3. Imprinting in Prader-Willi and Angelman syndromes;Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics;2005-11-15
4. SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome;Human Genetics;2004-05-01
5. RNA hairpins in noncoding regions of human brain and Caenorhabditis elegans mRNA are edited by adenosine deaminases that act on RNA;Proceedings of the National Academy of Sciences;2002-06-04
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