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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 25, 2010
Epilepsy caused by CDKL5 mutationsMaija Castrén, Eija Gaily, Carola Tengström, et al.Human Genetics|November 5, 2003
Identification of two AGTR2 mutations in male patients with non-syndromic mental retardationTero Ylisaukko-oja, Karola Rehnström, Raija Vanhala, et al.American Journal of Medical Genetics. Part A|December 4, 2004
MECP2 mutation analysis in patients with mental retardationTero Ylisaukko-Oja, Karola Rehnström, Raija Vanhala, et al.Nature|September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.Pageof 1