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Researcher
Inge Vereecke
Profile
Projects
Publications
Activities
Awards & Distinctions
4
Results
2015
Flexible, scalable, and efficient targeted resequencing on a benchtop sequencer for variant detection in clinical practice
Kim De Leeneer
Jan Hellemans
Wouter Steyaert
Steve Lefever
Inge Vereecke
Eveline Debals
Brecht Crombez
Machteld Baetens
Mattias Van Heetvelde
Frauke Coppieters
et al.
A1
Journal Article
in
HUMAN MUTATION
2015
2010
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients
Kristien Hoornaert
Inge Vereecke
Chantal Dewinter
Thomas Rosenberg
Frits A Beemer
Juliaan Leroy
Laila Bendix
Erik Björck
Maryse Bonduelle
Odile Boute
et al.
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2010
2008
Genotype and phenotype of Stickler syndrome caused by mutations in the COL2A1 gene
Kristien Hoornaert
Chantal Dewinter
Inge Vereecke
Paul Coucke
Geert Mortier
A2
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2008
2006
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene
Kristien Hoornaert
Chantal Dewinter
Inge Vereecke
FA BEEMER
W COURTENS
A FRYER
H FRYSSIRA
M LEES
A MULLNER-EIDENBOCK
DL RIMOIN
et al.
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
2006