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Sarah Waller

Showing results (21-30 of 22) with videos related to

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Orphanet Journal of Rare Diseases|September 16, 2016
The role of small in-frame insertions/deletions in inherited eye disorders and how structural modelling can help estimate their pathogenicityPanagiotis I Sergouniotis, Stephanie J Barton, Sarah Waller, et al.
Investigative Ophthalmology & Visual Science|January 28, 2017
Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early FeatureRachel L Taylor, Mark T Handley, Sarah Waller, et al.
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Showing results (21-30 of 22) with videos related to

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You have reached the last page of results.This site can display upto 22 results.
Orphanet Journal of Rare Diseases|September 16, 2016
The role of small in-frame insertions/deletions in inherited eye disorders and how structural modelling can help estimate their pathogenicityPanagiotis I Sergouniotis, Stephanie J Barton, Sarah Waller, et al.
Investigative Ophthalmology & Visual Science|January 28, 2017
Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early FeatureRachel L Taylor, Mark T Handley, Sarah Waller, et al.
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