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CEP89 is required for mitochondrial metabolism and neuronal function in man and fly. [electronic resource] by
- van Bon, Bregje W M
- Oortveld, Merel A W
- Nijtmans, Leo G
- Fenckova, Michaela
- Nijhof, Bonnie
- Besseling, Judith
- Vos, Melissa
- Kramer, Jamie M
- de Leeuw, Nicole
- Castells-Nobau, Anna
- Asztalos, Lenke
- Viragh, Erika
- Ruiter, Mariken
- Hofmann, Falko
- Eshuis, Lillian
- Collavin, Licio
- Huynen, Martijn A
- Asztalos, Zoltan
- Verstreken, Patrik
- Rodenburg, Richard J
- Smeitink, Jan A
- de Vries, Bert B A
- Schenck, Annette
Producer: 20140131
In:
Human molecular genetics vol. 22
Availability: No items available.
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GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila. [electronic resource] by
- 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
- Isidor, Bertrand
- Le Caignec, Cédric
- Lorino, Elsa
- Asztalos, Zoltan
- Koolen, David A
- Vissers, Lisenka E L M
- Schenck, Annette
- Kleefstra, Tjitske
Producer: 20140218
In:
Journal of medical genetics vol. 50
Availability: No items available.
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