Onderzoeker
Griet Van Buggenhout
- Disciplines:Genetica, Systeembiologie, Medische beeldvorming en therapie, Moleculaire en celbiologie, Andere paramedische wetenschappen
Affiliaties
- Departement Menselijke Erfelijkheid (Departement)
Lid
Vanaf1 dec 2000 → Heden
Publicaties
21 - 30 van 36
- Social cognition and underlying cognitive mechanisms in children with an extra X chromosome: a comparison with autism spectrum disorder(2014)
Auteurs: S van Rijn, L Stockmann, Griet Van Buggenhout, C van Ravenswaaij-Arts, H Swaab
Pagina's: 459 - 467 - Presenting symptoms in adults with the 22q11 deletion syndrome(2014)
Auteurs: Annick Vogels, Griet Van Buggenhout, Ann Swillen, Hilde Van Esch, Thomy de Ravel de l'Argentière, Koenraad Devriendt
Pagina's: 157 - 162 - Neuropsychopathology in 7 patients with the 22q13 deletion syndrome: presence of bipolar disorder and progressive loss of skills(2012)
Auteurs: Hilde Van Esch, Thomy de Ravel de l'Argentière, Jean-Pierre Frijns, Griet Van Buggenhout, Annick Vogels, Koenraad Devriendt, Ann Swillen
Pagina's: 14 - 20 - Adults with Down syndrome - health/care considerations for health professionals(2012)
Auteurs: Griet Van Buggenhout
Pagina's: 56 - 61 - Health problems in children with Down syndrome(2012)
Auteurs: Griet Van Buggenhout
Pagina's: 14 - 19 - Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood(2012)
Auteurs: Koenraad Devriendt, Jeroen Breckpot, Jean-Pierre Frijns, Hilde Peeters, Griet Van Buggenhout, Hilde Van Esch, Bea Maes, Ann Swillen
Pagina's: 135 - 148 - Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter(2011)
Auteurs: Griet Van Buggenhout, Jean-Pierre Frijns
Pagina's: 1833 - 47 - Wolf-Hirschhorn Syndrome Due to Pure and Translocation Forms of Monosomy 4p16.1 → pter(2011)
Auteurs: Griet Van Buggenhout, Jean-Pierre Frijns
Pagina's: 1833 - 1847 - Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations(2010)
Auteurs: Ellen Denayer, Koenraad Devriendt, Thomy de Ravel de l'Argentière, Griet Van Buggenhout, Inge Francois, Raf Sciot, Jean-Pierre Frijns, Eric Legius
Pagina's: 242 - 252 - Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations(2010)
Auteurs: Ellen Denayer, Koenraad Devriendt, Thomy de Ravel de l'Argentière, Griet Van Buggenhout, Eric Smeets, Inge Francois, Yves Sznajer, Margarita Craen, George Leventopoulos, Léon Mutesa, et al.
Pagina's: 242 - 252