De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch-Reference-Cited by-同舟云学术

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De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

Published:2000-05 Issue:1 Volume:25 Page:74-78
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Bielinska Beata,Blaydes Susan M.,Buiting Karin,Yang Tao,Krajewska-Walasek Malgorzata,Horsthemke Bernhard,Brannan Camilynn I.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0500_74.pdf

Reference29 articles.

1. Holm, V.A. et al. Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics 91, 398–402 ( 1993).

2. Nicholls, R.D., Saitoh, S. & Horsthemke, B. Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 14, 194–200 (1998).

3. Jong, M.T. et al. A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region. Hum. Mol. Genet. 8, 783– 793 (1999).

4. MacDonald, H.R. & Wevrick, R. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum. Mol. Genet. 6, 1873–1878 (1997).

5. Boccaccio, I. et al. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Hum. Mol. Genet . 8, 2497–2505 ( 1999).

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