Ubiquitous expression and imprinting of Snrpn in the mouse
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00355641.pdf
Reference21 articles.
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2. Bartolomei, M.S., Zemel, S., Tilghman, S.M. (1991). Parental imprinting of the mouse H19 gene. Nature 351, 153?155.
3. Cattanach, B.M., Barr, J.A., Evans, E.P., Burtenshaw, M., Beechey, C.V., Leff, S.E., Brannan, C.I., Copeland, N.G., Jenkins, Jones, J. (1992). A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nature Genet. 2, 270?274.
4. DeChiara, T.M., Robertson, E.J., Efstratiadis, A. (1991). Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849?859.
5. Giddings, S.J., King, C.D., Harman, K.W., Flood, J.F., Carnaghi, L.R. (1994). Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting. Nature Genet. 6, 310?313.
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