E. Jenkins

Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2)

B. Grisart, H. Stewart, G. Mancini, 2015, Clinical genetics.

Genetically guided precision medicine clinical decision support tools: a systematic review

G. Fiol, G. Del Fiol, M. Williams, 2023, medRxiv.

Genome sequencing identifies a non‐coding variant in the MCDR1 locus as a cause of macular dystrophy

P. Sergouniotis, G. Black, J. Ellingford, 2017, Clinical & experimental ophthalmology.