Article
[Identification of Y chromosome material in an XX male by means of fluorescent in situ hybridization].
Ugeskrift for laeger - 16 Nov 1992
Brandt C A, Hindkjaer J, Strømkjaer H, Christensen M F, Kølvraa S
Abstract excerpt
This article describes a case of 46,XX male, the most frequent form of sex reversal syndromes in humans. A method of identifying Y chromosome material in these and other patients with structural chromosomal abnormalities involving chromosome Y is given. Chromosomes from a phenotypically normal male child without any congenital malformation, where prenatal diagnosis revealed the female karyotype 46,XX, were...
Topics
- Adult
- DNA Probes
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Phenotype
- Prenatal Diagnosis
- Sex Chromosome Aberrations
- Sister Chromatid Exchange
- X Chromosome
