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Author/Creator Nillesen, Willy M

1. Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability. Issue 12 (15th October 2011)

Authors:
Willemsen, Marjolein H; Vallès, Astrid; Kirkels, Laurens A M H; Mastebroek, Mathilde; Olde Loohuis, Nikkie; Kos, Aron; Wissink-Lindhout, Willemijn M; de Brouwer, Arjan P M; Nillesen, Willy M; Pfundt, Rolph; Holder-Espinasse, Muriel; Vallée, Louis; Andrieux, Joris; Coppens-Hofman, Marjolein C; Ren...
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 12(2011)
Page Start:
810
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila. Issue 8 (4th May 2013)

Authors:
Willemsen, Marjolein H; Nijhof, Bonnie; Fenckova, Michaela; Nillesen, Willy M; Bongers, Ernie M H F; Castells-Nobau, Anna; Asztalos, Lenke; Viragh, Erika; van Bon, Bregje W M; Tezel, Emre; Veltman, Joris A; Brunner, Han G; de Vries, Bert B A; de Ligt, Joep; Yntema, Helger G; van Bokhoven, Hans; I...
Journal:
Journal of medical genetics
Issue:
Volume 50:Issue 8(2013)
Page Start:
507
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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