Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31.

類似資料

• HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.
  著者:: Carpten, J, 等
  出版事項: (2002)
• Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene.
  著者:: Cavaco, B, 等
  出版事項: (2004)
• Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31.
  著者:: Williamson, C, 等
  出版事項: (1999)
• Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999)
  著者:: Williamson, C, 等
  出版事項: (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))
  著者:: Williamson, C, 等
  出版事項: (1999)