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Thorax|March 26, 2005
Association of tumour necrosis factor alpha variants with the CF pulmonary phenotypeJ Yarden, D Radojkovic, K De Boeck, et al.
Pediatric Pulmonology|February 17, 2001
European Epidemiologic Registry of Cystic Fibrosis (ERCF): comparison of major disease manifestations between patients with different classes of mutationsC Koch, H Cuppens, M Rainisio, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Limited expansion of the (CAG)n repeat of the Huntington gene: a premutation (?)E Legius, H Cuppens, H Dierick, et al.
European Journal of Human Genetics : EJHG|December 7, 2000
Recommendations for quality improvement in genetic testing for cystic fibrosis. European Concerted Action on Cystic FibrosisE Dequeker, H Cuppens, J Dodge, et al.
Human Genetics|September 1, 1990
Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian familiesH Cuppens, E Legius, P Cabello, et al.
The Journal of Clinical Investigation|February 7, 1998
Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutationH Cuppens, W Lin, M Jaspers, et al.
Human Mutation|March 25, 1999
Mutation analysis in adenylosuccinate lyase deficiency: eight novel mutations in the re-evaluated full ADSL coding sequenceS Marie, H Cuppens, M Heuterspreute, et al.
Facts, Views & Vision in Obgyn|March 16, 2016
Art meets science: The Cosmopolitan Chicken Research ProjectA Stinckens, A Vereijken, E Ons, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
New clinical diagnostic procedures for cystic fibrosis in EuropeK De Boeck, N Derichs, I Fajac, et al.
Leukemia|June 18, 2011
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratoriesA Kohlmann, H-U Klein, S Weissmann, et al.
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