Molecular Genetic Findings in Prader-Willi Syndrome
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-0-387-33536-0_3.pdf
Reference76 articles.
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2. Bielinska B, Blaydes SM, Buiting K, et al. De novo deletions of the SNRPN exon 1 region in early human and mouse embryos result in a paternal to maternal imprint switch. Nature Genetics. 2000;25:74–78.
3. Bittel DC, Kibiryeva N, Talebizadeh Z, Butler MG. Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD. Journal of Medical Genetics. 2003;40:568–574.
4. Bittel DC, Kibiryeva N, Talebizadeh Z, Driscoll DJ, Butler MG. Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. Genomics. 2005;85:85–91.
5. Boccaccio I, Glatt-Deeley H, Watrin F, Roeckel N, Lalande M, Muscatelli F. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Human Molecular Genetics. 1999;8:2497–2505.
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