Prenatal diagnosis of androgen insensitivity

This publication has 6 references indexed in Scilit:

• Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene*
  Clinical Endocrinology, 2010
• Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome.
  Archives of Disease in Childhood, 1993
• Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome
  Human Molecular Genetics, 1992
• Cloning of Human Androgen Receptor Complementary DNA and Localization to the X Chromosome
  Science, 1988
• Molecular Cloning of Human and Rat Complementary DNA Encoding Androgen Receptors
  Science, 1988
• Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse.
  Proceedings of the National Academy of Sciences, 1981