Showing 1 - 4 results of 4 for search 'Cianferotti, L' Skip to content
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  • Cianferotti, L
Showing 1 - 4 results of 4 for search 'Cianferotti, L', query time: 0.02s Refine Results
  1. 1
    Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13.

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

    Published 1999
    Journal article
  2. 2
    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: relevance to familial benign hypocalciuric hypercalcaemia type 3.

    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:... by Hannan, F, Nesbit, M, Turner, J, Stacey, J, Cianferotti, L, Christie, P, Conigrave, A, Whyte, M, Thakker, R

    Published 2010
    Journal article
  3. 3
    Hypoparathyroidism: genetics and diagnosis

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

    Published 2022
    Journal article
  4. 4
    Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.

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

    Published 2003
    Journal article

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