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Neuropediatrics|June 10, 2005
Mitochondrial dysfunction in a patient with Joubert syndromeE Morava, A Dinopoulos, H Y Kroes, et al.Translational Psychiatry|September 23, 2015
Long-term consequences of chronic fluoxetine exposure on the expression of myelination-related genes in the rat hippocampusY Kroeze, D Peeters, F Boulle, et al.Neurology|January 13, 2010
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathiesM Lommel, S Cirak, T Willer, et al.Human Molecular Genetics|July 1, 1994
Cloning and characterization of the human choroideremia geneH van Bokhoven, J A van den Hurk, L Bogerd, et al.Human Genetics|October 5, 2016
Tooth agenesis and orofacial clefting: genetic brothers in arms?M Phan, F Conte, K D Khandelwal, et al.Clinical Genetics|June 26, 2002
De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastiaT Kleefstra, H G Yntema, A R Oudakker, et al.Human Molecular Genetics|July 1, 1994
Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patientsH van Bokhoven, M Schwartz, S Andréasson, et al.Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.Journal of Medical Genetics|October 23, 1998
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26H G Yntema, B C Hamel, A P Smits, et al.Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
The Opitz syndrome gene product, MID1, associates with microtubulesS Schweiger, J Foerster, T Lehmann, et al.Pageof 7