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Genetic Alliance UK
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UK
Mitochondrial Disease Priority Setting Partnership
research
Resetting the model
policy
Patient Charter on Newborn Screening
policy
genome sequencing and the nhs
research
CoOrdiNated Care Of Rare Diseases (CONCORD)
research
THE NICE TECHNOLOGY APPRAISAL PROGRAMME: OUR RESPONSE
policy
Responses to Parliamentary Inquiries: Brexit and Genome Editing
parliamentary
Understanding genome editing
research
Pledge For Patients 2017
policy
Genomics and genome-editing inquiry evidence
parliamentary
Pledge for Patients 2015-16
uk
Talking about genome editing
research
Response to the Caldicott Review
policy
The ethics of non invasive prenatal testing
policy
Research on non-invasive prenatal testing
research
Obstacles to patients gaining access to advanced therapies
policy
Brexit: the impact on rare disease
policy
The benefits of EU membership for our community
policy
Hidden Costs of Rare Disease Project
research
Cancer patients’ views on genome sequencing
research
Public perspectives on neuro-enhancement
research
Developing genetics training for primary care practitioners
eu
HRA UK policy framework for health and social care research
policy
My Condition, My DNA
policy
Genome Editing: What does it mean for patients?
policy
The Genomics Conversation
research
Consultation on non invasive prenatal testing
policy
Mitochondrial donation regulation consultation
policy
Use of animals in medical research
research
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