blog
John Chevers
Since 2001 there has been a voluntary moratorium in the UK precluding the use of genetic information for insurance purposes, except in specific circumstances.
Mark Kroese
Hilary Burton
Philippa Brice
Ron Zimmern
Alison Hall
Leila Luheshi
Lucia von Bredow
Sobia Raza
Gurdeep Sagoo
Charlotte Warren-Gash
Tom Finnegan
Susmita Chowdhury
consultation response
case study
report
PHG Foundation were commissioned to evaluate this pilot genetic services project in Birmingham..
Probable benefits, harms and costs of expanding newborn screening
Laura Blackburn
Examining the impact of routine testing using whole genome sequencing