Showing results (41-50 of 510) with videos related to
Sort By:
Pageof 51
Human Genetics|May 1, 1988
Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresisJ Morreau, M Sinaasappel, B A Oostra, et al.Biochimica Et Biophysica Acta|October 27, 1981
Terminal strand-switching of E. coli RNA polymerase transcribing a truncated DNA fragmentB A Oostra, A C Arnberg, G Ab, et al.Mental Retardation and Developmental Disabilities Research Reviews|March 3, 2004
The fragile X syndrome: from molecular genetics to neurobiologyRob Willemsen, Ben A Oostra, Gary J Bassell, et al.Journal of Medical Genetics|August 3, 2000
Twin sisters, monozygotic with the fragile X mutation, but with a different phenotypeR Willemsen, R Olmer, Y De Diego Otero, et al.Journal of Bacteriology|December 1, 1981
Enhancement of ribosomal ribonucleic acid synthesis by deoxyribonucleic acid gyrase activity in Escherichia coliB A Oostra, A J van Vliet, G Ab, et al.Journal of Virology|July 1, 1986
In vitro mutagenesis of the putative membrane-binding domain of polyomavirus middle-T antigenW Markland, S H Cheng, B A Oostra, et al.American Journal of Medical Genetics|May 20, 1999
Learning and memory in the FMR1 knockout mouseG S Fisch, H K Hao, C Bakker, et al.Neuroreport|March 25, 1998
No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndromeO Steward, C E Bakker, P J Willems, et al.Ophthalmic Paediatrics and Genetics|March 1, 1993
High symmetric anisometropia in monozygotic twinsP T De Jong, B A Oostra, J T De FaberJournal of Medical Genetics|May 1, 1993
Guidelines for the diagnosis of fragile X syndrome. National Fragile X FoundationB A Oostra, P B Jacky, W T Brown, et al.Pageof 51