Rapid prenatal diagnosis of aneuploidy from uncultured amniotic fluid cells using five-colour fluorescencein situ hybridization

This publication has 31 references indexed in Scilit:

• Prenatal diagnosis by in situ hybridization on uncultured amniocytes: Reduced sensitivity and potential risk of misdiagnosis in blood‐stained samples
  Prenatal Diagnosis, 1993
• Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype
  Human Molecular Genetics, 1992
• Impact of prenatal testing on maternal-fetal bonding: Chorionic villus sampling versus amniocentesis
  American Journal of Obstetrics and Gynecology, 1991
• Early prenatal diagnosis
  Prenatal Diagnosis, 1991
• Clinical applications of fluorescence in situ hybridization
  Genetic Analysis: Biomolecular Engineering, 1991
• Rapid metaphase and interphase detection of radiation‐induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization
  Cytometry, 1990
• Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes
  Human Genetics, 1988
• Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84
  Human Genetics, 1986
• Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21
  Cytogenetic and Genome Research, 1986
• Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocenteses
  Prenatal Diagnosis, 1984