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Anemia
Volume 2012 (2012), Article ID 865170, 6 pages
http://dx.doi.org/10.1155/2012/865170
Research Article

A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites

1Department of Clinical Genetics, VU University Medical Center, P.O. Box 7057, 1007 MB Amsterdam, The Netherlands
2Department of Pediatrics and Child Health, University of Manitoba, 675 McDermot Avenue, Winnipeg MB, Canada R3E 0V9
3Department of Cardiac Sciences, St. Boniface General Hospital, 405 Tache Avenue, Winnipeg MB, Canada R2H 2A6
4Medical Diagnostic Center Amstelland, P.O. Box 8018, 1180 LA Amstelveen, The Netherlands
5Department of Pediatrics, VU University Medical Center, P.O. Box 7057, 1007 MB Amsterdam, The Netherlands
6Department of Pediatric Oncology/Hematology, Erasmus MC, Sophia Children’s Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands
7Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, 6120 Executive Boulevard, 1Executive Plaza South, Room 7020, Rockville, MD 20852-7231, USA

Received 9 January 2012; Accepted 22 March 2012

Academic Editor: Henri J. van de Vrugt

Copyright © 2012 Yne de Vries et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Yne de Vries, Nikki Lwiwski, Marieke Levitus, et al., “A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites,” Anemia, vol. 2012, Article ID 865170, 6 pages, 2012. doi:10.1155/2012/865170