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...
Những tác giả chính: | 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 |
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Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
1999
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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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