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Phenogenon: Gene to Phenotype Associations for Rare Genetic Diseases
View ORCID ProfileCian Murphy, View ORCID ProfileIsmail Moghul, Nikolas Pontikos, Phenopolis consortium, UK Inherited Retinal Dystrophy consortium, UCLex consortium, Jing Yu
doi: https://doi.org/10.1101/367292
Cian Murphy
1UCL Genetics Institute, University College London, London WC1E 6BT, UK
2Warwick Medical School, University of Warwick, Coventry CV4 7AL, UK
Ismail Moghul
3UCL Cancer Institute, University College London, London WC1E 6DD, UK
Nikolas Pontikos
1UCL Genetics Institute, University College London, London WC1E 6BT, UK
4Institute of Ophthalmology, University College London, London EC1V 9EL, UK
5Moorfields Eye Hospital, London EC1V 2PD, UK
Jing Yu
6Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK

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Posted July 11, 2018.
Phenogenon: Gene to Phenotype Associations for Rare Genetic Diseases
Cian Murphy, Ismail Moghul, Nikolas Pontikos, Phenopolis consortium, UK Inherited Retinal Dystrophy consortium, UCLex consortium, Jing Yu
bioRxiv 367292; doi: https://doi.org/10.1101/367292
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