Research Explorer

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Researcher

Inge Vereecke

Awards & Distinctions

4 Results

2015

Flexible, scalable, and efficient targeted resequencing on a benchtop sequencer for variant detection in clinical practice

Kim De LeeneerJan HellemansWouter SteyaertSteve LefeverInge VereeckeEveline DebalsBrecht CrombezMachteld BaetensMattias Van HeetveldeFrauke Coppieters et al.

A1 Journal Article in HUMAN MUTATION

2010

Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients

Kristien HoornaertInge VereeckeChantal DewinterThomas RosenbergFrits A BeemerJuliaan LeroyLaila BendixErik BjörckMaryse BonduelleOdile Boute et al.

A1 Journal Article in EUROPEAN JOURNAL OF HUMAN GENETICS

2008

Genotype and phenotype of Stickler syndrome caused by mutations in the COL2A1 gene

Kristien HoornaertChantal DewinterInge VereeckePaul CouckeGeert Mortier

A2 Journal Article in EUROPEAN JOURNAL OF HUMAN GENETICS

2006

The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene

Kristien HoornaertChantal DewinterInge VereeckeFA BEEMERW COURTENSA FRYERH FRYSSIRAM LEESA MULLNER-EIDENBOCKDL RIMOIN et al.

A1 Journal Article in JOURNAL OF MEDICAL GENETICS