A paternal–specific methylation imprint marks the alleles of the mouse H19 gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0495-407.pdf
Reference40 articles.
1. Efstratiadis, A. Parental imprinting of autosomal mammalian genes. Cur. Opin. Genet. Devel. 4, 265–280 (1994).
2. Solter, D. Differential imprinting and expression of maternal and paternal genomes. A. Rev. Genet. 22, 127–146 (1988).
3. DeChiara, T.M., Robertson, E.J. & Efstratiadis, A. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849–859 (1991).
4. Leff, S.E. et al. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nature Genet. 2, 259–264 (1992).
5. Giddings, S.J., King, C.D., Harman, K.W., Flood, J.F. & Carnaghi, L.R. Allele specific inactivation of insulin 1 and 2 in the mouse yolk sac indicates imprinting. Nature Genet. 6, 310–313 (1994).
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