Development and progression of nephropathy in type 2 diabetes: the United Kingdom Prospective Diabetes Study (UKPDS 64). von Adler, A, Stevens, R, Manley, SE, Bilous, R, Cull, C, Holman, R

Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia. von Bilous, R, Murty, G, Parkinson, D, Thakker, R, Coulthard, MG, Burn, J, Mathias, D, Kendall-Taylor, P

GATA3 haplo-insufficiency causes human HDR syndrome. von Van Esch, H, Groenen, P, Nesbit, M, Schuffenhauer, S, Lichtner, P, Vanderlinden, G, Harding, B, Beetz, R, Bilous, R, Holdaway, I, Shaw, N, Fryns, J, Van de Ven, W, Thakker, R, Devriendt, K