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How is it used in the NHS
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About
Introduction to the GMS
What is genomics?
How is it used in the NHS
About the Genomic Medicine Service
Our GLH
Our GMSA
Meet the team
Clinical Genetic
Our Work
GLH
Pathway transformation
ctDNA
JBRCA
SCD
Generation study
Networks of Excellence
Prenatal genomic medicine
Mainstreaming
Nursing and midwifery
Pharmacy
Mental health
Primary care
Our successes
100k Genomes
Transformation Projects
Research
For healthcare professionals
Genetic Test Ordering
National Genomic Test Directories
Request / Find a Test Tool
Whole Genome Sequencing
Consent
Turn-around times
Test order forms
Sending a Sample
FAQs
Education and training
Training and Resources Catalogue
Curated Collections
For our people and patients
Genomics and my healthcare
Genomics and my family
Our panel
Resources
News and events
Our events calendar
NT GMS News
Careers
Genomics careers
Work for us
Contact
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Spinal muscular atrophy type 1 rare mutation testing
July 6, 2023 10:52 am
Published by
robhern
Adult onset hereditary spastic paraplegia
10:52 am
Published by
robhern
Childhood onset hereditary spastic paraplegia
10:52 am
Published by
robhern
Adult onset leukodystrophy
10:52 am
Published by
robhern
Paroxysmal central nervous system disorders
10:52 am
Published by
robhern
Early onset or syndromic epilepsy
10:52 am
Published by
robhern
Childhood onset dystonia, chorea or related movement disorder
10:52 am
Published by
robhern
Adult onset dystonia, chorea or related movement disorder
10:52 am
Published by
robhern
Hereditary ataxia with onset in childhood
10:52 am
Published by
robhern
Adult onset neurodegenerative disorder
10:52 am
Published by
robhern
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