Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome. by Reardon, W, Coffey, R, Chowdhury, T, Grossman, A, Jan, H, Britton, K, Kendall-Taylor, P, Trembath, R

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

Pendred syndrome--100 years of underascertainment? by Reardon, W, Coffey, R, Phelps, P, Luxon, L, Stephens, D, Kendall-Taylor, P, Britton, K, Grossman, A, Trembath, R

Radiological malformations of the ear in Pendred syndrome. by Phelps, P, Coffey, R, Trembath, R, Luxon, L, Grossman, AB, Britton, K, Kendall-Taylor, P, Graham, J, Cadge, B, Stephens, S, Pembrey, M, Reardon, W

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor. by Pearce, S, Williamson, C, Kifor, O, Bai, M, Coulthard, MG, Davies, M, Lewis-Barned, N, McCredie, D, Powell, H, Kendall-Taylor, P, Brown, E, Thakker, R

Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage. by Gausden, E, Coyle, B, Armour, J, Coffey, R, Grossman, A, Fraser, G, Winter, R, Pembrey, M, Kendall-Taylor, P, Stephens, D, Luxon, L, Phelps, P, Reardon, W, Trembath, R

Molecular analysis of the PDS gene in Pendred syndrome. by Coyle, B, Reardon, W, Herbrick, J, Tsui, L, Gausden, E, Lee, J, Coffey, R, Grueters, A, Grossman4, A, Phelps, P, Luxon, L, Kendall-Taylor, P, Scherer, S, Trembath, R