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European Reference Network Conference

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Mitochondrial Disease Priority Setting Partnership

research

Mitochondrial Disease Priority Setting Partnership

Protect European Reference Networks

eu

Protect European Reference Networks

Rare Musculoskeletal Diseases In Adulthood Priority Setting Partnership

research

Rare Musculoskeletal Diseases In Adulthood Priority Setting Partnership

genome sequencing and the nhs

research

genome sequencing and the nhs

CoOrdiNated Care Of Rare Diseases (CONCORD)

research

CoOrdiNated Care Of Rare Diseases (CONCORD)

Responses to Parliamentary Inquiries: Brexit and Genome Editing

parliamentary

Responses to Parliamentary Inquiries: Brexit and Genome Editing

Understanding genome editing

research

Understanding genome editing

Insurance and Genomics: Now

uk

Insurance and Genomics: Now

Pledge For Patients 2017

policy

Pledge For Patients 2017

Genomics and genome-editing inquiry evidence

parliamentary

Genomics and genome-editing inquiry evidence

The benefits of EU membership for our community

policy

The benefits of EU membership for our community

Treatment of Adrenal Insufficiency in Neonates and Infants (TAIN)

research

Treatment of Adrenal Insufficiency in Neonates and Infants (TAIN)

Resources about how medicines are developed (EUPATI)

research

Resources about how medicines are developed (EUPATI)

Cancer patients’ views on genome sequencing

research

Cancer patients’ views on genome sequencing

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Genetic Alliance UK provides the secretariat for the following parliamentary groups on Rare, Genetic and Undiagnosed Conditions:

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