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Research | 19 November 2006
Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion
- Eric.Legius@uz.kuleuven.ac.be
- Thomas De Raedt
- , Matthew Stephens
- , Ine Heyns
- , Hilde Brems
- , Daisy Thijs
- , Ludwine Messiaen
- , Karen Stephens
- , Conxi Lazaro
- , Katharina Wimmer
- , Hildegard Kehrer-Sawatzki
- , Dominique Vidaud
- , Lan Kluwe
- , Peter Marynen
- & Eric Legius
Nature Genetics 38 , 1419–1423

Rights & permissionsfor article Conservation of hotspots for recombination in low-copy repeats associated with the <i>NF1</i> microdeletion . Opens in a new window.
Research | 1 January 2003
PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning
- Eric.Legius@med.kuleuven.ac.be
- Els Schollen
- , Gert Matthijs
- , Marc Gewillig
- , Jean-Pierre Fryns
- & Eric Legius
European Journal of Human Genetics 11 , 85–88

Rights & permissionsfor article <i>PTPN11</i> mutation in a large family with Noonan syndrome and dizygous twinning . Opens in a new window.
Research | 13 August 2014
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies
- Eric.Legius@uzleuven.be
- Thomas De Raedt
- , Eline Beert
- , Eric Pasmant
- , Armelle Luscan
- , Hilde Brems
- , Nicolas Ortonne
- , Kristian Helin
- , Jason L. Hornick
- , Victor Mautner
- , Hildegard Kehrer-Sawatzki
- , Wade Clapp
- , James Bradner
- , Michel Vidaud
- , Meena Upadhyaya
- , Eric Legius
- & Karen Cichowski
Nature 514 , 247–251

Rights & permissionsfor article PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies . Opens in a new window.
Research | 19 August 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype
- Eric.Legius@uz.kuleuven.be
- Hilde Brems
- , Magdalena Chmara
- , Mourad Sahbatou
- , Ellen Denayer
- , Koji Taniguchi
- , Reiko Kato
- , Riet Somers
- , Ludwine Messiaen
- , Sofie De Schepper
- , Jean-Pierre Fryns
- , Jan Cools
- , Peter Marynen
- , Gilles Thomas
- , Akihiko Yoshimura
- & Eric Legius
Nature Genetics 39 , 1120–1126

Rights & permissionsfor article Germline loss-of-function mutations in <i>SPRED1</i> cause a neurofibromatosis 1–like phenotype . Opens in a new window.

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