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Eur J Hum Genet. 2014 Mar;22(3). doi: 10.1038/ejhg.2013.132. Epub 2013 Jul 3.

Clinical utility gene card for: Beckwith-Wiedemann Syndrome.

Author information

1
Department of Human Genetics, University Hospital, RWTH Aachen, Aachen, Germany.
2
Department of Genetics and Molecular Pathology, Monash Medical Centre, Clayton, Australia.
3
INGEMM, Instituto de Genética Médica y Molecular, Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCII, Madrid, Spain.
4
Department of Epigenetics, Faculty of Medicine, University of Southampton, Wessex Regional Genetics Laboratory, Salisbury Health Care Trust, Salisbury, UK.
5
Department of Medical Genetics, University of Cambridge Clinical School, Addenbrooke's Hospital Treatment Centre, Cambridge, UK.
6
Department of Clinical Genetics, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
7
Hôpital Trousseau, INSERM U938, UPMC, Paris 6, Explorations fonctionnelles endocriniennes, Paris, France.
8
Centre for Paediatric and Adolescent Medicine, University Medical Centre Mainz, Germany.
9
Seconda Università degli Studi di Napoli, Institute of Genetics and Biophysics - ABT, Napoli, Italy.
10
Department of Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
11
Department of Paediatrics and Genome Biology Program, Hospital for Sick Children and Institute of Medical Science, University of Toronto, Toronto, Canada.
PMID:
23820480
PMCID:
PMC3925261
DOI:
10.1038/ejhg.2013.132
[Indexed for MEDLINE]
Free PMC Article

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