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Surgery: Official Journal of the Society of University Surgeons, Central Surgical Association, and the American Association of Endocrine Surgeons, ISSN 0039-6060, 2014, Volume 156, Issue 6, pp. 1315 - 1325
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2002, Volume 32, Issue 4, pp. 676 - 680
Journal Article
Internal Medicine, ISSN 0918-2918, 2018, Volume 57, Issue 6, pp. 841 - 844
We herein report the case of a young woman who was diagnosed with primary hyperparathyroidism and in whom genetic testing confirmed a diagnosis of... 
HRPT2/CDC73 | hyperparathyroidism | hyperparathyroidism-jaw tumor syndrome | younger age | Hyperparathyroidism-jaw tumor syndrome | Hyperparathyroidism | Younger age | MEDICINE, GENERAL & INTERNAL | MUTATIONS | Jaw | Life expectancy | Life span | Surgery | Genetic testing | Diagnosis | Parathyroidectomy | Age | Genetic screening | HRPT2 | CDC73 | Case Report
Journal Article
Journal Article
World journal of surgery, ISSN 0364-2313, 09/2019, pp. 1 - 9
Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare disease caused by CDC73 germline mutations, with familial primary hyperparathyroidism (pHPT),... 
Jaw | Benign | Health risks | Imaging techniques | Exploration | Risk | Malignancy | Parathyroidectomy | Neoplasms | Surgery | Neck | Mutation | Lesions | Position (location) | Localization | Parathyroid | Hyperparathyroidism | Tumors | Thyroid
Journal Article
Oncogene, ISSN 0950-9232, 07/2017, Volume 36, Issue 28, pp. 4025 - 4036
Journal Article
Journal Article
Internal Medicine, ISSN 0918-2918, 2018
We herein report the case of a young woman who was diagnosed with primary hyperparathyroidism and in whom genetic testing confirmed a diagnosis of... 
HRPT2/CDC73 | hyperparathyroidism | hyperparathyroidism-jaw tumor syndrome | younger age
Journal Article
BMC medical genetics, ISSN 1471-2350, 09/2017, Volume 18, Issue 1, pp. 99 - 1
Following publication of the original article [1], the authors identified the following errors in the scientific content: p.4, para. 3: “(1 tablet/10 mL RIPA)”... 
Jaw | Clonal deletion | Exons | Hyperparathyroidism
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 07/2017, Volume 23, Issue 13, pp. e123 - e132
Children and adolescents who present with neuroendocrine tumors are at extremely high likelihood of having an underlying germline predisposition for the... 
PARATHYROID CARCINOMA | PITUITARY-ADENOMA | PRACTICE GUIDELINE | GERM-LINE MUTATIONS | FAMILIAL HYPERPARATHYROIDISM | ONCOLOGY | FUNCTIONAL-CHARACTERIZATION | MEDULLARY-THYROID CARCINOMA | RET PROTOONCOGENE MUTATIONS | TYPE-1 MEN1 | PARAFIBROMIN IMMUNOREACTIVITY | Fibroma - diagnosis | Hyperparathyroidism - diagnosis | Adenoma - epidemiology | Adenoma - genetics | Humans | Multiple Endocrine Neoplasia - genetics | Hyperparathyroidism - epidemiology | Germ-Line Mutation - genetics | Multiple Endocrine Neoplasia - diagnosis | Multiple Endocrine Neoplasia Type 2b - genetics | Jaw Neoplasms - epidemiology | Fibroma - epidemiology | Hyperparathyroidism - genetics | Tumor Suppressor Proteins - genetics | Child | Multiple Endocrine Neoplasia Type 2b - diagnosis | Adenoma - diagnosis | Genetic Predisposition to Disease | Multiple Endocrine Neoplasia - epidemiology | Risk Factors | Proto-Oncogene Proteins - genetics | Fibroma - genetics | Multiple Endocrine Neoplasia Type 2b - epidemiology | Adolescent | Jaw Neoplasms - diagnosis | Jaw Neoplasms - genetics | Proto-Oncogene Proteins c-ret - genetics | Adolescence | Jaw | Disorders | Surveillance | Multiple endocrine neoplasia | Surgery | Genetics | Diagnostic systems | Children | Adolescents | Hyperparathyroidism | Tumors | Cancer | Neuroendocrine tumors | Multiple Endocrine Neoplasia (MEN) 1 | RET | Hyperparathyroid-Jaw Tumor Syndromes | CDKN1B | germline | 2A, 2B, 4 | surveillance | CDC73 | MEN1
Journal Article