Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations ofCDC73gene in Chinese

Frequent Large GermlineHRPT2Deletions in a French National Cohort of Patients With Primary Hyperparathyroidism

(2013) Léopoldine Bricaire et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Mutation analysis in two Chinese families with multiple endocrine neoplasia type 1

(2012) Zhang Wen et al.   Arquivos Brasileiros de Endocrinologia e Metabologia

Ectopic Parathyroid Glands and their Anatomical, Clinical and Surgical Implications

(2012) G. Noussios et al.   EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES

Novel HRPT2/CDC73 Gene Mutations and Loss of Expression of Parafibromin in Chinese Patients with Clinically Sporadic Parathyroid Carcinomas

(2012) Ou Wang et al.   PLoS One

Identification of the first germline HRPT2 whole-gene deletion in a patient with primary hyperparathyroidism

(2011) Rita Domingues et al.   CLINICAL ENDOCRINOLOGY

Multiple endocrine neoplasia type 1 in Japan: establishment and analysis of a multicentre database

(2011) Akihiro Sakurai et al.   CLINICAL ENDOCRINOLOGY

Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors

(2011) Wai Kwan Siu et al.   Familial Cancer

Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome family

(2011) Alberto Cascón et al.   GENES CHROMOSOMES & CANCER

HRPT2-related familial isolated hyperparathyroidism: could molecular studies direct the surgical approach?

(2010) Leticia G. Silveira et al.   Arquivos Brasileiros de Endocrinologia e Metabologia

MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27Kip1 and p18INK4C) mutations

(2010) Marianthi Georgitsi   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

A novel mutation of the MEN1 gene in a Chinese kindred with multiple endocrine neoplasia type 1

(2010) Lei Xu et al.   ENDOCRINE JOURNAL

Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors

(2010) Paul J. Newey et al.   HUMAN MUTATION

Sporadic and MEN1-Related Primary Hyperparathyroidism: Differences in Clinical Expression and Severity

(2009) Cristina Eller-Vainicher et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Parafibromin - functional insights

(2009) P. J. Newey et al.   JOURNAL OF INTERNAL MEDICINE

Hyperparathyroidism–jaw tumor syndrome: a report of three large kindred

(2009) Maurizio Iacobone et al.   LANGENBECKS ARCHIVES OF SURGERY

The extent of parathyroidectomy for HRPT2-related hyperparathyroidism

(2009) Maurizio Iacobone et al.   SURGERY

Parathyroid Carcinoma: Etiology, Diagnosis, and Treatment

(2009) Takahiro Okamoto et al.   WORLD JOURNAL OF SURGERY

Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism

(2008) G. Masi et al.   ENDOCRINE-RELATED CANCER

Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations

(2008) Marta S. Sarquis et al.   SURGERY

Re: Familial hyperparathyroidism: Surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations

(2008) Vito Guarnieri et al.   SURGERY