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The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred. [electronic resource] by
- Cavaco, B M
- Barros, L
- Pannett, A A
- Ruas, L
- Carvalheiro, M
- Ruas, M M
- Krausz, T
- Santos, M A
- Sobrinho, L G
- Leite, V
- Thakker, R V
Producer: 20010524
In:
QJM : monthly journal of the Association of Physicians vol. 94
Availability: No items available.
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7.
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Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions. [electronic resource] by
- Cavaco, B M
- Domingues, R
- Bacelar, M C
- Cardoso, H
- Barros, L
- Gomes, L
- Ruas, M M A
- Agapito, A
- Garrão, A
- Pannett, A A J
- Silva, J L
- Sobrinho, L G
- Thakker, R V
- Leite, V
Producer: 20020711
In:
Clinical endocrinology vol. 56
Availability: No items available.
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8.
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Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. [electronic resource] by
- Bradley, K J
- Cavaco, B M
- Bowl, M R
- Harding, B
- Cranston, T
- Fratter, C
- Besser, G M
- Conceição Pereira, M
- Davie, M W J
- Dudley, N
- Leite, V
- Sadler, G P
- Seller, A
- Thakker, R V
Producer: 20060721
In:
Clinical endocrinology vol. 64
Availability: No items available.
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9.
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Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. [electronic resource] by
- Bradley, K J
- Hobbs, M R
- Buley, I D
- Carpten, J D
- Cavaco, B M
- Fares, J E
- Laidler, P
- Manek, S
- Robbins, C M
- Salti, I S
- Thompson, N W
- Jackson, C E
- Thakker, R V
Producer: 20050214
In:
Journal of internal medicine vol. 257
Availability: No items available.
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10.
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Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. [electronic resource] by
- Pannett, A A J
- Kennedy, A M
- Turner, J J O
- Forbes, S A
- Cavaco, B M
- Bassett, J H D
- Cianferotti, L
- Harding, B
- Shine, B
- Flinter, F
- Maidment, C G H
- Trembath, R
- Thakker, R V
Producer: 20030613
In:
Clinical endocrinology vol. 58
Availability: No items available.
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11.
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Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31. [electronic resource] by
- Williamson, C
- Cavaco, B M
- Jauch, A
- Dixon, P H
- Forbes, S
- Harding, B
- Holtgreve-Grez, H
- Schoell, B
- Pereira, M C
- Font, A P
- Loureiro, M M
- Sobrinho, L G
- Santos, M A
- Thakker, R V
- Jausch, A
Producer: 19990308
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 14
Availability: No items available.
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12.
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HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. [electronic resource] by
- Carpten, J D
- Robbins, C M
- Villablanca, A
- Forsberg, L
- Presciuttini, S
- Bailey-Wilson, J
- Simonds, W F
- Gillanders, E M
- Kennedy, A M
- Chen, J D
- Agarwal, S K
- Sood, R
- Jones, M P
- Moses, T Y
- Haven, C
- Petillo, D
- Leotlela, P D
- Harding, B
- Cameron, D
- Pannett, A A
- Höög, A
- Heath, H
- James-Newton, L A
- Robinson, B
- Zarbo, R J
- Cavaco, B M
- Wassif, W
- Perrier, N D
- Rosen, I B
- Kristoffersson, U
- Turnpenny, P D
- Farnebo, L-O
- Besser, G M
- Jackson, C E
- Morreau, H
- Trent, J M
- Thakker, R V
- Marx, S J
- Teh, B T
- Larsson, C
- Hobbs, M R
Producer: 20030117
In:
Nature genetics vol. 32
Availability: No items available.
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