Familial benign hypercalcemia--from clinical description to molecular genetics.

Lignende værker

• Familial benign hypocalciuric hypercalcemia--from the clinic to the calcium sensor.
  af: Strewler, G J
  Udgivet: (1994)
• Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.
  af: Heath, H, et al.
  Udgivet: (1993)
• Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.
  af: Pearce, S H, et al.
  Udgivet: (1995)
• Benign familial haematuria in children from the Jewish communities of Israel: clinical and genetic studies.
  af: Eisenstein, B, et al.
  Udgivet: (1979)
• Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.
  af: Lloyd, S E, et al.
  Udgivet: (1999)