[Diagnosis of minor chromosome modifications by molecular cytogenetics]

Ann Genet. 1989;32(4):204-10.
[Article in French]

Abstract

Chromosomal in situ hybridization with radioactive probes allows the detection of single copy DNA segments of very small size. In two phenotypically normal individuals, classical chromosomal analysis revealed a small partial deletion of chromosome 18 short arm. In situ hybridization of probe D18S3, located at 18p13, showed in both instances a balanced reciprocal translocation: 46,XY,t(5;18) (p153;p112) and 46,XX,t(18;22)(p111;p11), respectively.

Publication types

  • English Abstract

MeSH terms

  • Abortion, Habitual / genetics*
  • Chromosome Deletion
  • Chromosomes, Human, Pair 18
  • Chromosomes, Human, Pair 22
  • Chromosomes, Human, Pair 5
  • DNA Probes
  • Female
  • Humans
  • Karyotyping / methods*
  • Nucleic Acid Hybridization
  • Pedigree
  • Pregnancy
  • Translocation, Genetic

Substances

  • DNA Probes