Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.

Ítems similars

• LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
  per: Trump, D, et al.
  Publicat: (1995)
• LINKAGE STUDIES IN A KINDRED WITH HYPOCALCIURIC HYPERCALCEMIA AND INCREASING SERUM PARATHYROID-HORMONE LEVELS INDICATE GENETIC-HETEROGENEITY
  per: Trump, D, et al.
  Publicat: (1993)
• Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis.
  per: Pearce, S, et al.
  Publicat: (1996)
• Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13.
  per: Cianferotti, L, et al.
  Publicat: (1999)
• Familial benign hypercalcaemia, Oklahoma variant (FBHok): Localisation to chromosome 19q13.
  per: Lloyd, SE, et al.
  Publicat: (1997)