The hyperparathyroidism-jaw tumour (HPT-JT) syndrome
The hyperparathyroidsim-jaw tumour (HPT-JT) syndrome is an autosomal dominant disorder characterised by the occurence of parathyroid tumours, which may be carcinomas in approximately 15% of patients, and ossifying fibromes, that usually affect the maxilla and/or mandible. More than 15% of HPT-JT pat...
Հիմնական հեղինակներ: | Bradley, K, Thakker, R |
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Ձևաչափ: | Journal article |
Լեզու: | English |
Հրապարակվել է: |
2006
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Նմանատիպ նյութեր
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Clinical and genetic studies of the hyperparathyroidism-jaw tumor syndrome (HPT-JT) in a kindred from Portugal.
: Cavaco, B, և այլն
Հրապարակվել է: (1999) -
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors.
: Newey, P, և այլն
Հրապարակվել է: (2010) -
A two-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family: clinical presentations, pathological characteristics and genetic analysis: a case report
: Dun Yang, և այլն
Հրապարակվել է: (2022-09-01) -
Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family
: Vito Guarnieri, և այլն
Հրապարակվել է: (2017-09-01) -
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome.
: Bradley, K, և այլն
Հրապարակվել է: (2005)