Androgen insensitivity in man: evidence for genetic heterogeneity.

Ítems similars

• Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity.
  per: Meyer, W J, et al.
  Publicat: (1975)
• 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)
• Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity.
  per: Witkop, C J, et al.
  Publicat: (1970)
• Androgen insensitivity syndrome.
  per: Williams, D M, et al.
  Publicat: (1993)
• 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.
  per: Lubahn, D B, et al.
  Publicat: (1989)