M. Williams

Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome.

M. Ognjanović, R. Gilbert, M. Saleem, 2013, Clinical journal of the American Society of Nephrology : CJASN.

Clinical and genetic analysis of patients with cystinuria in the United Kingdom.

D. Thwaites, J. Sayer, G. Welsh, 2015, Clinical journal of the American Society of Nephrology : CJASN.

Comparative multiplex dosage analysis detects whole exon deletions at the phenylalanine hydroxylase locus

S. Ring, L. Tyfield, M. Gable, 2003, Human mutation.

A case of congenital central hypoventilation syndrome in a three‐generation family with non‐polyalanine repeat PHOX2B mutation

A. Donaldson, T. Hilliard, M. Williams, 2014, Pediatric pulmonology.