Identification of new Wilms tumour predisposition genes: an exome sequencing study-Reference-Cited by-同舟云学术

Identification of new Wilms tumour predisposition genes: an exome sequencing study

Published:2019-05 Issue:5 Volume:3 Page:322-331
ISSN:2352-4642
Container-title:The Lancet Child & Adolescent Health
language:en
Short-container-title:The Lancet Child & Adolescent Health

Author:

Mahamdallie Shazia,Yost Shawn,Poyastro-Pearson Emma,Holt Esty,Zachariou Anna,Seal Sheila,Elliott Anna,Clarke Matthew,Warren-Perry Margaret,Hanks Sandra,Anderson John,Bomken Simon,Cole Trevor,Farah Roula,Furtwaengler Rhoikos,Glaser Adam,Grundy Richard,Hayden James,Lowis Steve,Millot Frédéric,Nicholson James,Ronghe Milind,Skeen Jane,Williams Denise,Yeomanson Daniel,Ruark Elise,Rahman Nazneen

Publisher

Elsevier BV

Subject

Developmental and Educational Psychology,Pediatrics, Perinatology, and Child Health

Reference30 articles.

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3. Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour;Hanks;Nat Commun,2014

4. Mutations in the transcriptional repressor REST predispose to Wilms tumor;Mahamdallie;Nat Genet,2015

5. Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor;Scott;Nat Genet,2008

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