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Central and South Genomics Service
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Evaluating Familial Screening After a Hypertrophic Cardiomyopathy-Related Sudden Cardiac Death
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Central and South Genomics Service
Main Menu
Home
About us
Menu Toggle
Who we are
Our team
Contact us
For Healthcare professionals
Menu Toggle
Overview
How to request a test
Rare disease
Cancer
Education and Training
Research
Menu Toggle
LR CASe Detectives
For patients
Menu Toggle
Overview
Frequently Asked Questions
Support groups
How to get involved
Transformation projects
Menu Toggle
ctDNA
Equity of access in R65 testing
Evaluating Familial Screening After a Hypertrophic Cardiomyopathy-Related Sudden Cardiac Death
Facilitating WGS in ophthalmology clinics
Familial breast cancer
Familial Hypercholesterolaemia (FH)
Genomic Tumour Advisory Boards (GTABs)
Genomics Pathology Accelerator Project (GPAP)
Genomic testing for paediatric endocrinology
Genseize
Lynch syndrome
Mendelscan
Monogenic Inflammatory Bowel Disease
Non Invasive Prenatal Testing 2
Preconception Optimised Exome Testing (POET):
RNA sequencing
Sudden Unexpected Death
Whole genome sequencing for cancer
News
Menu Toggle
Events
Patient Stories
Contact us
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