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Human Genome Variation|October 25, 2019
Breakpoint junction features of seven DMD deletion mutationsNiall P Keegan, Steve D Wilton, Sue FletcherSocial Science & Medicine (1982)|September 2, 2008
Understanding, embracing, rejecting: Women's negotiations of disability constructions and categorizations after becoming chronically illValorie A Crooks, Vera Chouinard, Robert D WiltonBiochemical Pharmacology|May 9, 1997
Compartmentalisation and characteristics of a Ca2+-dependent phospholipase A2 in human colon mucosaE Lamura, K Hillier, A Kinkaid, et al.Frontiers in Genetics|June 27, 2022
Corrigendum: Analysis of Pathogenic Pseudoexons Reveals Novel Mechanisms Driving Cryptic SplicingNiall P Keegan, Steve D Wilton, Sue FletcherCurrent Opinion in Neurology|November 10, 2000
Gene therapy and molecular approaches to the treatment of hereditary muscular disordersS Fletcher, S D Wilton, J M HowellTrends in Molecular Medicine|June 9, 2015
The emperor's new dystrophin: finding sense in the noiseS D Wilton, R N Veedu, S FletcherFrontiers in Genetics|February 10, 2022
Analysis of Pathogenic Pseudoexons Reveals Novel Mechanisms Driving Cryptic SplicingNiall P Keegan, Steve D Wilton, Sue FletcherInorganic Chemistry|August 21, 2001
Two-, three-, and four-coordination at gold(I) supported by the bidentate selenium ligand [Ph2P(Se)NP(Se)Ph2](-)J D Wilton-Ely, A Schier, H SchmidbaurCellular and Molecular Life Sciences : CMLS|April 28, 2012
Regulation of eukaryotic gene expression by the untranslated gene regions and other non-coding elementsLucy W Barrett, Sue Fletcher, Steve D WiltonPrenatal Diagnosis|August 1, 1993
Verification of carrier status for Becker muscular dystrophy from analysis of a blighted ovumS D Wilton, J Goldblatt, N G LaingPageof 24