Publications by authors named "Ivy Jennes"

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Identification and functional characterization of the human EXT1 promoter region.
Ivy Jennes, Monia Zuntini, Kirsten Mees, Ajay Palagani, Elena Pedrini

Gene· January 2012

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Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factors.
Elena Pedrini, Ivy Jennes, Morena Tremosini, Annamaria Milanesi, Marina Mordenti

J Bone Joint Surg Am· December 2011

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Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 multiple osteochondromas families.
Ivy Jennes, Danielle de Jong, Kirsten Mees, Pancras C W Hogendoorn, Karoly Szuhai

BMC Med Genet· June 2011

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Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients.
Károly Szuhai, Ivy Jennes, Danielle de Jong, Judith V M G Bovée, Malgorzata Wiweger

Hum Mutat· February 2011

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Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
Ivy Jennes, Elena Pedrini, Monia Zuntini, Marina Mordenti, Sahila Balkassmi

Hum Mutat· December 2009

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Mutation screening of EXT1 and EXT2 by denaturing high-performance liquid chromatography, direct sequencing analysis, fluorescence in situ hybridization, and a new multiplex ligation-dependent probe amplification probe set in patients with multiple osteochondromas.
Ivy Jennes, Mark M Entius, Els Van Hul, Alessandro Parra, Luca Sangiorgi

J Mol Diagn· January 2008

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