Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity

Ítems similars

• Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity
  Publicat: (1990)
• Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome.
  per: Brown, T R, et al.
  Publicat: (1988)
• Complete androgen insensitivity syndrome
  per: Tančić-Gajić Milina, et al.
  Publicat: (2015-01-01)
• Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity.
  per: Meyer, W J, et al.
  Publicat: (1975)
• Androgen insensitivity in man: evidence for genetic heterogeneity.
  per: Amrhein, J A, et al.
  Publicat: (1976)