Associated Papers
A Familial Case of a Whole Germline CDC73 Deletion Discordant for Primary Hyperparathyroidism.
Hatabu N et al.
Hormone Research in Paediatrics, 2019
Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma.
Cardoso L et al.
Human Mutation, 2017
Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas.
Haven CJ et al.
Clinical Endocrinology, 2007
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors.
Cetani F et al.
The Journal of Clinical Endocrinology and Metabolism, 2004
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