Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications
Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications
About this item
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Author / Creator
Warner, J , Epstein, M , Sweet, A , Singh, D , Burgess, J , Stranks, S , Hill, P , Perry-Keene, D , Learoyd, D , Robinson, B , Birdsey, P , Mackenzie, E , Teh, B T , Prins, J B and Cardinal, J
Publisher
London: BMJ Publishing Group Ltd
Journal title
Language
English
Formats
Publication information
Publisher
London: BMJ Publishing Group Ltd
Subjects
More information
Scope and Contents
Contents
Familial hyperparathyroidism is not uncommon in clinical endocrine practice. It encompasses a spectrum of disorders including multiple endocrine neoplasia types 1 (MEN1) and 2A, hyperparathyroidism-jaw tumour syndrome (HPT-JT), familial hypocalciuric hypercalcaemia (FHH), and familial isolated hyperparathyroidism (FIHP). Distinguishing among the fi...
Alternative Titles
Full title
Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications
Authors, Artists and Contributors
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Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1735699
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1735699
Other Identifiers
ISSN
0022-2593,1468-6244
E-ISSN
1468-6244
DOI
10.1136/jmg.2003.016725
