Resultats de la cerca - Mathilde Mastebroek
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1
Experiences of patients with intellectual disabilities and carers in GP health information exchanges: a qualitative study per Mathilde Mastebroek, Jenneken Naaldenberg, Francine A. van den Driessen Mareeuw, Antoine L. M. Lagro-Janssen, H. M. J. van Schrojenstein Lantman‐de Valk
Publicat 2016Artigo -
2
Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability per Marjolein H. Willemsen, Astrid Vallès, Laurens A. M. H. Kirkels, Mathilde Mastebroek, Nikkie Olde Loohuis, Aron Kos, W.M. Wissink-Lindhout, Arjan P.M. de Brouwer, Willy M. Nillesen, Rolph Pfundt, Muriel Holder‐Espinasse, Louis Vallée, Joris Andrieux, Marjolein C. Coppens‐Hofman, Hanneke Rensen, Ben C.J. Hamel, Hans van Bokhoven, Armaz Aschrafi, Tjitske Kleefstra
Publicat 2011Artigo -
3
Update on Kleefstra Syndrome per Marjolein H. Willemsen, Anneke T. Vulto‐van Silfhout, Willy M. Nillesen, W.M. Wissink-Lindhout, Hans van Bokhoven, N. Philip, Elizabeth Berry‐Kravis, Usha Kini, Conny M.A. van Ravenswaaij‐Arts, Barbara Delle Chiaie, A. Micheil Innes, Gunnar Houge, T Kosonen, Kirsten Cremer, Madeleine Fannemel, Asbjørg Stray‐Pedersen, William Reardon, Jaakko Ignatius, Katherine Lachlan, Clotilde Mircher, P.T.J.M. Helderman van den Enden, Mathilde Mastebroek, Petra E. Cohn‐Hokke, Helger G. Yntema, Séverine Drunat, Tjitske Kleefstra
Publicat 2011Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Intellectual disability
Medicine
Phenotype
Psychiatry
Bioinformatics
DPYD
Economic growth
Economics
Enhancer
Family medicine
Genotype
Gerontology
Health care
Health information
Hypotonia
Microdeletion syndrome
Microphthalmia-associated transcription factor
Nursing
Pediatrics
Pharmacogenetics
Qualitative research
Social science
Sociology
Transcription factor
microRNA