Genetic technology for the study of rare diseases CPD Archived

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Lucy Raymond lectures on recent advances in the genetic technology used for the study of rare diseases. She discusses the mutational mechanisms for rare diseases and the developments in sequencing technology, using case studies to explore the way this technology works in practice.

This lecture was part of an event called "Rare disease workshop" at The Royal Society of Medicine in London.

Date of lecture: 5th July 2013 

This video is available for iPad via Safari.

Length: 00:31:15

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51:06

Professor Sir Mark Walport, Director of the Wellcome Trust.

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28:42

Dr Daniel Gale, UCL & West London Renal and Transplant Centre.

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51:48

Dr Carlo Croce, Comprehensive Cancer Center, USA.

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21:16

Jonathan O'Halloran & Elaine Warburton, QuantuMDx Group.

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53:34

Sir John Burn, Professor of Clinical Genetics, Newcastle University.

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22:12

Fiona Karet, Professor of Nephrology, University of Cambridge. 

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31:15

Lucy Raymond, Reader in Neurogenetics, University of Cambridge.

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57:20
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45:43

Elizabeth Blackburn, Biological Researcher, The University of California.

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