WES

31 January 2022

Cerebral palsy can be genetic

26 February 2021

Largest Middle East GWAS reveals clinically relevant variants

19 February 2021

WES uncovers mutations for rare paediatric diseases

19 November 2020

Early results from the UK Biobank Exome Sequencing Consortium

29 October 2020

Clinical utility of exome sequencing in pregnancy loss

Neuritogenesis genes confer risk for cerebral palsy

15 September 2020

Genetic modifiers impact long-term survival in sickle cell anaemia

Whole-exome sequencing as a tool to detect inborn errors of metabolism