Author/Creator: Poulson, Arabella V - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Poulson, Arabella V

1. Alternative splicing modifies the effect of mutations in COL11A1 and results in recessive type 2 Stickler syndrome with profound hearing loss. Issue 11 (6th August 2013)

Authors:: Richards, Allan J; Fincham, Gregory S; McNinch, Annie; Hill, David; Poulson, Arabella V; Castle, Bruce; Lees, Melissa M; Moore, Anthony T; Scott, John D; Snead, Martin P
Journal:: Journal of medical genetics
Issue:: Volume 50:Issue 11(2013)
Page Start:: 765
Record Type:: Journal Article
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2. Clinical characterisation and molecular analysis of Wagner syndrome. Issue 5 (11th October 2006)

Authors:: Meredith, Sarah P; Richards, Allan J; Flanagan, Declan W; Scott, John D; Poulson, Arabella V; Snead, Martin P
Journal:: British journal of ophthalmology
Issue:: Volume 91:Issue 5(2007)
Page Start:: 655
Record Type:: Journal Article
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3. Deep Intronic Sequence Variants in COL2A1 Affect the Alternative Splicing Efficiency of Exon 2, and May Confer a Risk for Rhegmatogenous Retinal Detachment. Issue 10 (21st August 2016)

Authors:: Spickett, Carl; Hysi, Pirro; Hammond, Chistopher J; Prescott, Alan; Fincham, Gregory S; Poulson, Arabella V; McNinch, Annie M; Richards, Allan J; Snead, Martin P
Journal:: Human mutation
Issue:: Volume 37:Issue 10(2016)
Page Start:: 1085
Record Type:: Journal Article
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