Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor-Reference-Cited by-同舟云学术

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

Published:2008-10-05 Issue:11 Volume:40 Page:1329-1334
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Scott Richard H, ,Douglas Jenny,Baskcomb Linda,Huxter Nikki,Barker Karen,Hanks Sandra,Craft Alan,Gerrard Mary,Kohler Janice A,Levitt Gill A,Picton Sue,Pizer Barry,Ronghe Milind D,Williams Denise,Cook Jackie A,Pujol Pascal,Maher Eamonn R,Birch Jillian M,Stiller Charles A,Pritchard-Jones Kathy,Rahman Nazneen

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.243.pdf

Reference30 articles.

1. Gicquel, C. et al. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nat. Genet. 37, 1003–1007 (2005).

2. Weksberg, R., Shuman, C. & Smith, A.C. Beckwith-Wiedemann syndrome. Am. J. Med. Genet. C. Semin. Med. Genet. 137, 12–23 (2005).

3. Scott, R.H., Stiller, C.A., Walker, L.L. & Rahman, N. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J. Med. Genet. 43, 705–715 (2006).

4. Little, S.E. et al. Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study. J. Clin. Oncol. 22, 4140–4146 (2004).

5. Reik, W. et al. Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2–H19 domain. Hum. Mol. Genet. 4, 2379–2385 (1995).

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