Winnie Courtens

Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion

Winnie Courtens, Dominique Grossman, Nadine Van Roy et al. · Human Genetics · 1998 · 94 citations

Life Sciences, Genetics, Molecular Genetics +13

Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.

Marc Abramowicz, Marc Andrien, E. Dupont et al. · Journal of Clinical Investigation · 1994 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics

Liesbeth Rooms, Edwin Reyniers, Wim Wuyts et al. · Clinical Genetics · 2005 · 69 citations

Medicine, Genetics, Molecular Genetics +15

Microduplication 22q11.2: A benign polymorphism or a syndrome with a very large clinical variability and reduced penetrance?—Report of two families

Winnie Courtens, Inge Schramme, Annick Laridon · American Journal of Medical Genetics Part A · 2008 · 69 citations

Life Sciences, Genetics, Molecular Genetics +14

A subterminal deletion of the long arm of chromosome 10: A clinical report and review

Winnie Courtens, Wim Wuyts, Liesbeth Rooms et al. · American Journal of Medical Genetics Part A · 2006 · 54 citations

Life Sciences, Genetics, Molecular Genetics +17