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Correspondence
Nature Genetics  37, 785 - 786 (2005)
doi:10.1038/ng0805-785

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

Dirk Prawitt1, 6, Thorsten Enklaar1, 6, Barbara Gärtner-Rupprecht1, Christian Spangenberg1, Ekkehart Lausch1, Dirk Reutzel1, Stephan Fees1, Maria Korzon2, Izabela Brozek3, Janusz Limon3, David E Housman4, Jerry Pelletier5 & Bernhard Zabel1

1  Children's Hospital, University of Mainz, Langenbeckstr. 1, D-55101 Mainz, Germany.

2  Medical University of Gdansk, Poland.

3  Department of Biology and Genetics, Medical University of Gdansk, Poland.

4  Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.

5  Department of Biochemistry and McGill Cancer Center, McGill University, Montreal, H3G 1Y6, Canada.

6  These authors contributed equally to this work.

Correspondence should be addressed to Dirk Prawitt prawitt@molgen.medizin.uni-mainz.de


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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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