Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15-Reference-Cited by-同舟云学术

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Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

Published:1995-04-01 Issue:4 Volume:9 Page:395-400
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Buiting Karin,Saitoh Shinji,Gross Stephanie,Dittrich Bärbel,Schwartz Stuart,Nicholls Robert D.,Horsthemke Bernhard

Publisher

Springer Science and Business Media LLC

Link

http://www.nature.com/articles/ng0495-395.pdf

Reference34 articles.

1. Nicholls, R.D. Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes. Curr. Opin. Genet. Dev. 3, 445–456 (1993).

2. Özcelik, T. et al. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nature Genet. 2, 265–269 (1992).

3. Glenn, C.C., Porter, K.A., Jong, M.T.C., Nicholls, R.D. & Driscoll, D.J. Functional imprinting and epigenetlc modification of the human SNRPN gene. Hum. molec. Genet. 2, 2001–2005 (1993).

4. Reed, M.L. & Left, S.E. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome. Nature Genet. 6, 163–167 (1994).

5. Sutcliffe, J.S. et al. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nature Genet. 8, 52–58 (1994).

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