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Nucleic Acids Research|September 11, 1982
Deletion loop mutagenesis: a novel method for the construction of point mutations using deletion mutantsD Kalderon, B A Oostra, B K Ely, et al.Human Genetics|July 11, 2002
Timing of the absence of FMR1 expression in full mutation chorionic villiRob Willemsen, Carola J M Bontekoe, Lies-Anne Severijnen, et al.The Biochemical Journal|December 1, 1990
Characterization of the human lysosomal alpha-glucosidase geneL H Hoefsloot, M Hoogeveen-Westerveld, A J Reuser, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|January 15, 2000
Perinatal cortical infarction within middle cerebral artery trunksP Govaert, E Matthys, A Zecic, et al.Trends in Molecular Medicine|September 25, 2010
Potential therapeutic interventions for fragile X syndromeJosien Levenga, Femke M S de Vrij, Ben A Oostra, et al.Human Molecular Genetics|February 28, 1998
In vitro reactivation of the FMR1 gene involved in fragile X syndromeP Chiurazzi, M G Pomponi, R Willemsen, et al.Developmental Medicine and Child Neurology|March 22, 2008
Prevalence, type, distribution, and severity of cerebral palsy in relation to gestational age: a meta-analytic reviewE Himpens, C Van den Broeck, A Oostra, et al.Neurogenetics|May 4, 2010
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindredGuido J Breedveld, Giovanni Fabbrini, Ben A Oostra, et al.Human Genetics|March 1, 1992
Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndromeJ O Van Hemel, B Eussen, E Wesby-van Swaay, et al.Molecular & General Genetics : MGG|January 1, 1981
A mutation in the RNA polymerase beta' subunit causing depressed ribosomal RNA synthesis in Escherichia coliB A Oostra, K Kok, A J Van Vliet, et al.Pageof 51