Two years' prospective experience using fluorescencein situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies

This publication has 14 references indexed in Scilit:

• PRENATAL DETECTION OF CHROMOSOME ANEUPLOIDIES BY FLUORESCENCE IN SITU HYBRIDIZATION: EXPERIENCE WITH 2000 UNCULTURED AMNIOTIC FLUID SAMPLES IN A PROSPECTIVE PRECLINICAL TRIAL
  Prenatal Diagnosis, 1997
• Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (Fish)
  Prenatal Diagnosis, 1994
• Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study
  Prenatal Diagnosis, 1994
• Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescencein situhybridization
  Prenatal Diagnosis, 1994
• Prenatal diagnosis by in situ hybridization on uncultured amniocytes: Reduced sensitivity and potential risk of misdiagnosis in blood‐stained samples
  Prenatal Diagnosis, 1993
• Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification
  Genomics, 1992
• Isolation of chromosome 21–specific yeast artificial chromosomes from a total human genome library
  Nature Genetics, 1992
• Is non-isotopic in situ hybridization finally coming of age?
  Nature, 1990
• Rapid detection of human chromosome 21 aberrations by in situ hybridization.
  Proceedings of the National Academy of Sciences, 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