Onderzoeker
Jan Vermeesch
- Trefwoorden:Algemene en logistieke diensten
Affiliaties
- Vrije Universiteit Brussel (Universiteit)
Lid
Vanaf1 jan 1987 → 31 dec 1987
Publicaties
1 - 10 van 12
- Genomewide copy number alteration screening of circulating plasma DNA(2019)
Auteurs: Lore Lenaerts, Pierre Vandenberghe, Nathalie Brison, Huiwen Che, Maria Neofytou, Magali Verheecke, Lies Leemans, Charlotte Maggen, Bart Dewaele, Luc Dehaspe, et al.
Pagina's: 85-95 - Recent developments in genetics and medically assisted reproduction(2018)
Auteurs: J.c. Harper, K Aittomäki, Pascal Borry, M C Cornel, Guido De Wert, W.j. Dondorp, J. Geraedts, Luca Gianaroli, K Ketterson, Ingeborg Liebaers, et al.
Pagina's: 12-33 - Recent developments in genetics and medically-assisted reproduction(2017)
Auteurs: J.c. Harper, K Aittomäki, Pascal Borry, M C Cornel, Guido De Wert, W Dondorp, J. Geraedts, Luca Gianaroli, K Ketterson, Ingeborg Liebaers, et al.
Pagina's: 1-20 - Abstracts of the 26th World Congress on Ultrasound in Obstetrics and Gynecology, Rome, Italy, 24-28 September 2016(2016)
Auteurs: J Muys, B Blaumeiser, K Janssens, C Bandelier, J Gatot, Jan Vermeesch, S Rombout, B Menten, B Pichon, K Van Den Bogaert, et al.
- Clinical implementation of NIPT - technical and biological challenges(2016)
Auteurs: PD Brady, Nathalie Brison, K. Bogaert, Thomy de Ravel, Haaike Peeters, Hilde Van Esch, Karel Devriendt, Eric Legius, Jan Vermeesch
Pagina's: 523-30 - Sporadic male patients with intellectual disability(2012)
Auteurs: Mala Isrie, G. Froyen, Karel Devriendt, J.p. Fryns, Jan Vermeesch, Hilde Van Esch
Pagina's: 577-85 - Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements(2010)
Auteurs: Boyan Dimitrov, Thomy De Ravel, Joris Van Driessche, C.e.m. De Die-Smulders, A Toutain, Jan Vermeesch, J.p. Fryns, Karel Devriendt, Ph. Debeer
Pagina's: 103-111 - Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome(2009)
Auteurs: I. Balikova, A-E Lehesjoki, K E Chandler, Jill Clayton-Smith, A-L Träskelin, J.p. Fryns, Jan Vermeesch
Pagina's: E845-54 - 17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction(2009)
Auteurs: B Grisart, L Willatt, A. Destrée, J.p. Fryns, K Rack, J. C. Rosenfeld, Jan Vermeesch, C. Verellen-Dumoulin, R Sandford
Pagina's: 524-30 - Further delineation of the 15q13 microdeletion and duplication syndromes(2009)
Auteurs: B W M van Bon, H C Mefford, B. Menten, D A Koolen, A J Sharp, W M Nillesen, J W Innis, C L Mercer, M Fichera, Helen Stewart, et al.
Pagina's: 511-23