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' tumorDirk 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 Zabel11
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 REFERENCES
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