Langerhans cell histiocytosis in children with congenital anomalies: A population-based record linkage study-Reference-Cited by-同舟云学术

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Langerhans cell histiocytosis in children with congenital anomalies: A population-based record linkage study

Published:2015-02 Issue:2 Volume:103 Page:157-160
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Salotti Jane A.¹,Tennant Peter W.G.¹,Windebank Kevin²,Rankin Judith¹

Affiliation:

1. Institute of Health & Society, Newcastle University; Baddiley-Clark Building, Richardson Road Newcastle upon Tyne United Kingdom

2. Northern Institute for Cancer Research, Newcastle University; Paul O'Gorman Building, Medical School, Framlington Place Newcastle upon Tyne United Kingdom

Funder

Newlife Foundation for Disabled Children

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bdra.23350/fullpdf

Reference22 articles.

1. Langerhans cell histiocytosis in children born 1982-2005 after in vitro fertilization;Åkefeldt;Acta Paediatr,2012

2. Associations between congenital malformations and childhood cancer. A register-based case-control study;Altmann;Br J Cancer,1998

3. Familial clustering of Langerhans cell histiocytosis;Aricò;Br J Haematol,1999

4. Recurrent BRAF mutations in Langerhans cell histiocytosis;Badalian-Very;Blood,2010

5. Minor anomalies in children with hematological malignancies;Citak;Pediatr Blood Cancer,2011

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