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

Ítems similars

• Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms.
  per: Tusié-Luna, M T, et al.
  Publicat: (1995)
• Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.
  per: Sinnott, P, et al.
  Publicat: (1990)
• Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.
  per: Amor, M, et al.
  Publicat: (1988)
• Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.
  per: Haglund-Stengler, B, et al.
  Publicat: (1991)
• Evidence for frequent gene conversion in the steroid 21-hydroxylase P-450(C21) gene: implications for steroid 21-hydroxylase deficiency.
  per: Higashi, Y, et al.
  Publicat: (1988)