Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups-Reference-Cited by-同舟云学术

Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups

Published:2016-07-15 Issue:9 Volume:170 Page:2248-2260
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Maas Saskia M.¹²,Vansenne Fleur³,Kadouch Daniel J. M.⁴,Ibrahim Abdulla⁵⁶,Bliek Jet⁷,Hopman Saskia⁸,Mannens Marcel M.⁷,Merks Johannes H. M.¹,Maher Eamonn R.⁵,Hennekam Raoul C.¹

Affiliation:

1. Department of Pediatrics; Academic Medical Center; Amsterdam The Netherlands

2. Department of Clinical Genetics; Academic Medical Center; Amsterdam The Netherlands

3. Department of Clinical Genetics; University Medical Center Groningen; Groningen The Netherlands

4. Department of Plastic Surgery; Academic Medical Center; Amsterdam The Netherlands

5. Department of Medical Genetics; University of Cambridge and NHR Cambridge Biomedical Research Centre; Cambridge United Kingdom

6. Department of Clinical Genetics; University of Dundee; Ninewells Hospital and Medical School; Dundee United Kingdom

7. Department of Clinical Genetics; DNA-Diagnostics Laboratory, Academic Medical Center; Amsterdam The Netherlands

8. Department of Genetics; University Medical Center; Utrecht The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference71 articles.

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2. Beckwith-Wiedemann and Russell-;Azzi;Curr Opin Endocrinol Obes,2014

3. Children at increased risk for Wilms tumor: Monitoring issues;Beckwith;J Pediatr,1998a

4. Nephrogenic rests and the pathogenesis of Wilms tumor: Developmental and clinical considerations;Beckwith;Am J Med Genet,1998b

5. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: Occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS;Bliek;Hum Mol Genet,2001

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