Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism.

Lignende værker

• Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients
  af: Ars, E, et al.
  Udgivet: (2003)
• Confirmation of a double-hit model for the NF1 gene in benign neurofibromas.
  af: Serra, E, et al.
  Udgivet: (1997)
• Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.
  af: Milà, M, et al.
  Udgivet: (1996)
• A clinical variant of neurofibromatosis type 1: familial spinal neurofibromatosis with a frameshift mutation in the NF1 gene.
  af: Ars, E, et al.
  Udgivet: (1998)
• The Relation of Germ Line Mosaicism to Somatic Mosaicism in Drosophila
  af: Lee, William R., et al.
  Udgivet: (1967)