Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31.
A Portuguese kindred with autosomal dominant isolated primary hyperparathyroidism (HPT) that was associated with parathyroid adenomas and carcinomas was investigated with the aim of determining the chromosomal location of this gene, designated HPTPort. Leukocyte DNA from 9 affected and 16 unaffected...
Hlavní autoři: | Williamson, C, Cavaco, B, Jauch, A, Dixon, P, Forbes, S, Harding, B, Holtgreve-Grez, H, Schoell, B, Pereira, M, Font, A, Loureiro, M, Sobrinho, L, Santos, M, Thakker, R, Jausch, A |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
1999
|
Podobné jednotky
-
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999)
Autor: Williamson, C, a další
Vydáno: (1999) -
Erratum: Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (Journal of Bone and Mineral Research (February 1999) 14 (230-239))
Autor: Williamson, C, a další
Vydáno: (1999) -
The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred.
Autor: Cavaco, B, a další
Vydáno: (2001) -
Clinical and genetic studies of the hyperparathyroidism-jaw tumor syndrome (HPT-JT) in a kindred from Portugal.
Autor: Cavaco, B, a další
Vydáno: (1999) -
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.
Autor: Bradley, K, a další
Vydáno: (2006)