Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13.

Eitemau Tebyg

• LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
  gan: Trump, D, et al.
  Cyhoeddwyd: (1995)
• Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.
  gan: Lloyd, SE, et al.
  Cyhoeddwyd: (1999)
• 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.
  gan: Trump, D, et al.
  Cyhoeddwyd: (1995)
• Familial benign hypercalcaemia, Oklahoma variant (FBHok): Localisation to chromosome 19q13.
  gan: Lloyd, SE, et al.
  Cyhoeddwyd: (1997)
• Identification of a second kindred with familial hypocalciuric hypercalcemia type 3 (FHH3) narrows localization to a <3.5 megabase pair region on chromosome 19q13.3.
  gan: Nesbit, M, et al.
  Cyhoeddwyd: (2010)