Brenda J. Barry
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Data Protection Basics for Local Community Groups, Non-Profits and Social Enterprises delivered by the Data Protection Commission, 23 September
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Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders
D.G.M. is a paid adviser to GlaxoSmithKline; Insitro; Variant Bio and Overtone Therapeutics and has received research support from AbbVie; Astellas; Biogen; BioMarin; Eisai; Merck; Microsoft; Pfizer and Sanofi-Genzyme; none of these activities are related to the work presented here. M.E.T. is provided with research reagents and/or resources from Microsoft; Illumina; Pacific Biosciences; and Ionis Pharmaceuticals; none of these are related to the work presented here.
Presence of Copy Number Variants Associated With Esotropia in Patients With Exotropia
Presence of Copy Number Variants Associated With Esotropia in Patients With Exotropia Key Points Question Are genetic risk factors for esotropia also risk factors for exotropia? Findings In this cross-sectional study including 234 individuals, genetic duplications associated with esotropia on chromosomes 2, 4, and 10 were found to be present in 1.7%, 3.0%, and 6.0%, respectively, of individuals with exotropia.
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