Utilisation of a cryptic non-canonical donor splice site of the gene encoding PARAFIBROMIN is associated with familial isolated primary hyperparathyroidism. par Bradley, K, Cavaco, B, Bowl, MR, Harding, B, Young, A, Thakker, R

Expression and function of the chemokine receptor CCR7 in thyroid carcinomas. par Sancho, M, Vieira, J, Casalou, C, Mesquita, M, Pereira, T, Cavaco, B, Dias, S, Leite, V

Expression of vascular endothelial growth factor (VEGF) and its receptors in thyroid carcinomas of follicular origin: a potential autocrine loop. par Vieira, J, Santos, S, Espadinha, C, Correia, I, Vag, T, Casalou, C, Cavaco, B, Catarino, A, Dias, S, Leite, V

Clinical and genetic studies of the hyperparathyroidism-jaw tumor syndrome (HPT-JT) in a kindred from Portugal. par Cavaco, B, Pannett, A, Barros, J, Ruas, L, Ruas, M, Leite, V, Sobrinho, L, Santos, M, Thakker, R

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene. par Cavaco, B, Guerra, L, Bradley, K, Carvalho, D, Harding, B, Oliveira, A, Santos, M, Sobrinho, L, Thakker, R, Leite, V

The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred. par Cavaco, B, Barros, L, Pannett, A, Ruas, L, Carvalheiro, M, Ruas, M, Krausz, T, Santos, M, Sobrinho, L, Leite, V, Thakker, R

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. par Bradley, K, Hobbs, MR, Buley, I, Carpten, J, Cavaco, B, Fares, J, Laidler, P, Manek, S, Robbins, C, Salti, I, Thompson, N, Jackson, C, Thakker, R

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. par Pannett, A, Kennedy, A, Turner, J, Forbes, SA, Cavaco, B, Bassett, J, Cianferotti, L, Harding, B, Shine, B, Flinter, F, Maidment, C, Trembath, R, Thakker, R

Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions. par Cavaco, B, Domingues, R, Bacelar, M, Cardoso, H, Barros, L, Gomes, L, Ruas, M, Agapito, A, Garrão, A, Pannett, A, Silva, J, Sobrinho, L, Thakker, R, Leite, V

Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999) par Williamson, C, Cavaco, B, Jauch, A, Dixon, P, Forbes, S, Harding, B, Holtgreve-Grez, H, Schoell, B, Pereira, M, Font, A, Loureiro, M, Sobrinho, L, Santos, M, Thakker, R

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. par Bradley, K, Cavaco, B, Bowl, MR, Harding, B, Cranston, T, Fratter, C, Besser, G, Conceição Pereira, M, Davie, M, Dudley, N, Leite, V, Sadler, G, Seller, A, Thakker, R

Erratum: Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (Journal of Bone and Mineral Research (February 1999) 14 (23... par Williamson, C, Cavaco, B, Jauch, A, Dixon, P, Forbes, S, Harding, B, Holtgreve-Grez, H, Schoell, B, Pereira, M, Font, A, Loureiro, M, Sobrinho, L, Santos, M, Thakker, R

Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31. par Williamson, C, Cavaco, B, Jauch, A, Dixon, P, Forbes, S, Harding, B, Holtgreve-Grez, H, Schoell, B, Pereira, M, Font, A, Loureiro, M, Sobrinho, L, Santos, M, Thakker, R, Jausch, A

Genomic profiling reveals mutational landscape in parathyroid carcinomas. par Pandya, C, Uzilov, A, Bellizzi, J, Lau, C, Moe, A, Strahl, M, Hamou, W, Newman, L, Fink, M, Antipin, Y, Yu, W, Stevenson, M, Cavaco, B, Teh, B, Thakker, R, Morreau, H, Schadt, E, Sebra, R, Li, S, Arnold, A, Chen, R