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B M Cavaco

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Clinical Endocrinology|February 21, 2006
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumoursK J Bradley, B M Cavaco, M R Bowl, et al.
Clinical Endocrinology|April 18, 2003
Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidismA A J Pannett, A M Kennedy, J J O Turner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 5, 1999
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31C Williamson, B M Cavaco, A Jauch, et al.
Nature Genetics|November 16, 2002
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndromeJ D Carpten, C M Robbins, A Villablanca, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Clinical Endocrinology|February 21, 2006
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumoursK J Bradley, B M Cavaco, M R Bowl, et al.
Clinical Endocrinology|April 18, 2003
Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidismA A J Pannett, A M Kennedy, J J O Turner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 5, 1999
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31C Williamson, B M Cavaco, A Jauch, et al.
Nature Genetics|November 16, 2002
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndromeJ D Carpten, C M Robbins, A Villablanca, et al.
Pageof 2