Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13. nork Cianferotti, L, Pannett, A, Whyte, M, Thakker, R

Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences:... nork Hannan, F, Nesbit, M, Turner, J, Stacey, J, Cianferotti, L, Christie, P, Conigrave, A, Whyte, M, Thakker, R

Hypoparathyroidism: genetics and diagnosis nork Mannstadt, M, Cianferotti, L, Gafni, RI, Giusti, F, Kemp, EH, Koch, CA, Roszko, KL, Yao, L, Guyatt, GH, Thakker, RV, Xia, W, Brandi, M

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. nork 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