The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0701_232.pdf
Reference49 articles.
1. Nicholls, R.D., Saitoh, S. & Horsthemke, B. Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 14, 194–200 (1998).
2. Jiang, Y., Tsai, T.-F., Bressler, J. & Beaudet, A.L. Imprinting in Angelman and Prader- Willi syndromes. Curr. Opin. Genet. Dev. 8, 334–342 (1998).
3. Mann, M.R. & Bartolomei, M.S. Towards a molecular understanding of Prader-Willi and Angelman syndromes. Hum. Mol. Genet. 8, 1867–1873 (1999).
4. Schulze, A. et al. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint. Nature Genet. 12, 452–454 (1996).
5. Sun, Y. et al. Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient. Hum. Mol. Genet. 5, 517–524 (1996).
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