Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

Lignende værker

• Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene
  af: Koppens, P, et al.
  Udgivet: (2003)
• Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.
  af: Collier, S, et al.
  Udgivet: (1989)
• Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms.
  af: Tusié-Luna, M T, et al.
  Udgivet: (1995)
• Frequent deletion and duplication of the steroid 21-hydroxylase genes.
  af: Werkmeister, J W, et al.
  Udgivet: (1986)
• 21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.
  af: Sinnott, P J, et al.
  Udgivet: (1989)