Article
Association of the Hind III polymorphism with the androgen receptor gene in partial androgen insensitivity syndrome.
Annales de genetique - 1 Jan 1991
Lobaccaro J M, Belon C, Ruiz-Pacheco R, Heinrichs C, Van Regemorter N, Terraza A, Sultan C
Abstract excerpt
Partial androgen insensitivity syndrome (PAIS) is an X-linked disorder resulting from defects in the intracellular androgen receptor (AR). The cloning of the AR cDNA has provided the molecular tools to identify gene abnormalities. Gene deletions being the exception in PAIS, prenatal diagnosis of...
Topics
- Alleles
- Deoxyribonuclease HindIII
- Female
- Genitalia, Male
- Humans
- Infant, Newborn
- Male
- Polymorphism, Restriction Fragment Length
- Receptors, Androgen
- Sex Differentiation
- Syndrome
- X Chromosome