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International Journal of Evidence-Based Healthcare|July 3, 2015
Guidance for conducting systematic scoping reviewsMicah D J Peters, Christina M Godfrey, Hanan Khalil, et al.Journal of Cell Science|May 1, 1989
Lithium ions induce prestalk-associated gene expression and inhibit prespore gene expression in Dictyostelium discoideumD J Peters, M M Van Lookeren Campagne, P J Van Haastert, et al.Human Genetics|June 1, 2000
Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISHV Bezrookove, K Hansson, M van der Burg, et al.Clinical Genetics|May 29, 2009
Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophyA T J M Helderman-van den Enden, R de Jong, J T den Dunnen, et al.American Journal of Medical Genetics|June 5, 1995
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)P E Taschner, N de Vos, J G Post, et al.Developmental Genetics|January 1, 1991
Control of cAMP-induced gene expression by divergent signal transduction pathwaysD J Peters, M Cammans, S Smit, et al.Clinical Genetics|May 11, 2007
Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposisM Nielsen, F J Hes, F M Nagengast, et al.Journal of Medical Genetics|April 3, 2004
Genomic imbalances in mental retardationM Kriek, S J White, M C Bouma, et al.Human Mutation|August 19, 2006
Duplications in the DMD geneS J White, A Aartsma-Rus, K M Flanigan, et al.Clinical Genetics|July 19, 2012
An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissectionY Hilhorst-Hofstee, A J H A Scholte, M E B Rijlaarsdam, et al.Pageof 24