A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a model.

Ítems similars

• Direct detection of point mutations by mismatch analysis: application to haemophilia B.
  per: Montandon, A J, et al.
  Publicat: (1989)
• Molecular pathology of haemophilia B.
  per: Green, P M, et al.
  Publicat: (1989)
• The Italian haemophilia B mutation database: a tool for genetic counselling, carrier detection and prenatal diagnosis
  per: Tagariello, Giuseppe, et al.
  Publicat: (2007)
• A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism.
  per: Tsang, T C, et al.
  Publicat: (1988)
• Haemophilia B: database of point mutations and short additions and deletions—third edition, 1992
  per: Giannelli, F., et al.
  Publicat: (1992)