Items where Division is "Faculties (pre 2018 reorg) > Faculty of Medicine (pre 2018 reorg) > Human Development & Health (pre 2018 reorg) > Human Genetics (pre 2018 reorg)
Current Faculties > Faculty of Medicine > Human Development and Health > Human Development & Health (pre 2018 reorg) > Human Genetics (pre 2018 reorg)
Human Development and Health > Human Development & Health (pre 2018 reorg) > Human Genetics (pre 2018 reorg)" and Year is 2017
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Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B) -
Chelsea S. Norman,
Luke O'Gorman,
Jane Gibson,
Reuben J. Pengelly,
Diana Baralle,
J. Arjuna Ratnayaka,
Helen Griffiths,
Matthew Rose-Zerilli,
Megan Ranger,
David Bunyan,
Helena Lee,
Rhiannon Page,
Tutte Newall,
Fatima Shawkat,
Christopher Mattocks,
Daniel Ward,
Sarah Ennis and
Jay E. Self
Type: Article
| 2017
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