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Series 2 Episode 4 - Newborn genome screening

Series
Centre for Personalised Medicine
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What sort of findings might we get from newborn genome screening? What might this mean for the NHS? Rachel Horton talks to Gabby Samuel and Lisa Ballard.

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Centre for Personalised Medicine

Series 2 Episode 3 - Sharing genetic results within families

Who does a genetic result belong to? What might help people to share genetic information with their relatives? We talk to Lisa Ballard and Anneke Lucassen.
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Centre for Personalised Medicine

Series 2 Episode 5 - Who's 'the patient' in genomic medicine?

We live our lives alongside others, and our decisions have consequences for those close to us - what does this mean for how we define 'the patient' in genomic medicine? Susie Weller talks to us about this issue.
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Episode Information

Series
Centre for Personalised Medicine
People
Rachel Horton
Gabrielle Samuel
Lisa Ballard
Keywords
genomics
bioethics
screening
public health
Evidence Based Medicine; Statistics; Medical Statistics; Uncertainty; Risk; Healthcare; Evidence Based Healthcare; Public Health; Primary Care
Department: Wellcome Trust Centre for Human Genetics
Date Added: 20/10/2022
Duration: 00:19:02

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