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European Journal of Neurology|May 24, 2011
NIPA1 mutation in complex hereditary spastic paraplegia with epilepsyK Svenstrup, R S Møller, J Christensen, et al.
Clinical Genetics|October 19, 2007
Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobeR S Møller, C P Hansen, G D Jackson, et al.
Clinical Genetics|May 1, 2008
Mowat-Wilson syndrome: an underdiagnosed syndrome?E Engenheiro, R S Møller, M Pinto, et al.
American Journal of Medical Genetics. Part A|July 13, 2012
Genetic studies in congenital anterior midline cervical cleftL P Jakobsen, P Pfeiffer, M Andersen, et al.
Clinical Genetics|October 13, 2017
Clinician's guide to genes associated with Rett-like phenotypes-Investigation of a Danish cohort and review of the literatureB Schönewolf-Greulich, A-M Bisgaard, R S Møller, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 1, 2019
Clinical and genetic spectrum of SCN2A-associated episodic ataxiaN Schwarz, T Bast, E Gaily, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 23, 2017
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugsC von Stülpnagel, M Ensslen, R S Møller, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
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