Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe

Hum Genet. 1989 Aug;83(1):88-92. doi: 10.1007/BF00274156.

Abstract

The relationship between Y-chromosome abnormalities and gonadal differentiation was investigated in six phenotypic females with a 46,XY karyotype and one patient with ambiguous genitalia secondary to apparently nonmosaic 46,XY mixed gonadal dysgenesis. No alterations were found in the Y chromosomes of six of these individuals by the use of either cytogenetic or molecular techniques. Cytogenetic analysis with high-resolution G-banding and Q-banding revealed a small deletion in the short arm of the Y chromosome in one female patient with some features of Turner syndrome. Southern hybridization with Y-specific probes showed a loss of DNA within deletion intervals 1, 2, and 3 of the Y chromosome. A new Y-chromosome-specific DNA probe that hybridizes to deletion interval 3 is described.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abnormalities, Multiple / genetics
  • Adolescent
  • Adult
  • Blotting, Southern
  • Child, Preschool
  • Chromosome Banding
  • Chromosome Deletion*
  • DNA Probes*
  • Female
  • Genetic Markers*
  • Gonadal Dysgenesis / genetics*
  • Gonadal Dysgenesis, 46,XY / genetics*
  • Gonadal Dysgenesis, Mixed / genetics
  • Humans
  • Infant, Newborn
  • Male
  • Polymorphism, Restriction Fragment Length
  • Y Chromosome*

Substances

  • DNA Probes
  • Genetic Markers