The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred.
The hyperparathyroidism-jaw tumour (HPT-JT) syndrome is an autosomal dominant disease characterized by the occurrence of parathyroid tumours and fibro-osseous tumours of the jaw bones. Some HPT-JT patients may also develop renal abnormalities, which include Wilms' tumours, hamartomas and polycy...
Үндсэн зохиолчид: | Cavaco, B, Barros, L, Pannett, A, Ruas, L, Carvalheiro, M, Ruas, M, Krausz, T, Santos, M, Sobrinho, L, Leite, V, Thakker, R |
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Формат: | Journal article |
Хэл сонгох: | English |
Хэвлэсэн: |
2001
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Ижил төстэй зүйлс
Ижил төстэй зүйлс
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Clinical and genetic studies of the hyperparathyroidism-jaw tumor syndrome (HPT-JT) in a kindred from Portugal.
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The hyperparathyroidism-jaw tumour (HPT-JT) syndrome
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Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome.
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Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31.
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Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999)
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