Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations

Author:

van de Putte RomyORCID,Wijers Charlotte H. W.,Reutter Heiko,Vermeulen Sita H.,Marcelis Carlo L. M.,Brosens Erwin,Broens Paul M. A.,Homberg Markus,Ludwig Michael,Jenetzky Ekkehart,Zwink Nadine,Sloots Cornelius E. J.,de Klein Annelies,Brooks Alice S.,Hofstra Robert M. W.,Holsink Sophie A. C.,van der Zanden Loes F. M.,Galesloot Tessel E.,Tam Paul Kwong-Hang,Steehouwer Marloes,Acuna-Hidalgo Rocio,Vorst Maartje van de,Kiemeney Lambertus A.,Garcia-Barceló Maria-Mercè,de Blaauw Ivo,Brunner Han G.,Roeleveld Nel,van Rooij Iris A. L. M.

Funder

Radboud Universitair Medisch Centrum

Bundesministerium für Bildung und Forschung, BMBF

Deutsche Forschungsgemeinschaft

Sophia Foundations

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference42 articles.

1. InternationalClearinghouse. Annual report 2014—International clearinghouse for birth defects surveillance and research. 2014.

2. Anorectal anomalies associated with or as part of other anomalies;A Cuschieri;Am J Med Genet,2002

3. Associated malformations in patients with anorectal anomalies;C Stoll;Eur J Med Genet,2007

4. Critical factors affecting quality of life of adult patients with anorectal malformations or Hirschsprung’s disease;EE Hartman;Am J Gastroenterol,2004

5. Maternal and paternal risk factors for anorectal malformations: a Dutch case-control study;IA van Rooij;Birth Defects Res A Clin Mol Teratol,2010

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