Prenatal diagnosis with use of fetal cells isolated from maternal blood: Five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21

This publication has 20 references indexed in Scilit:

• Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
  Nature Genetics, 1996
• Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum.
  Proceedings of the National Academy of Sciences, 1996
• Detection of Fetal Trisomies 21 and 18 From Maternal Blood Using Triple Gradient and Magnetic Cell Sorting
  American Journal of Reproductive Immunology, 1993
• Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers
  The Lancet, 1993
• First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood
  The Lancet, 1992
• Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry
  American Journal of Obstetrics and Gynecology, 1991
• Detection of single-copy fetal DNA sequence from maternal blood
  The Lancet, 1990
• Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood
  Blood, 1990
• Isolation of fetal DNA from nucleated erythrocytes in maternal blood.
  Proceedings of the National Academy of Sciences, 1990
• PRENATAL SEX DETERMINATION BY DNA AMPLIFICATION FROM MATERNAL PERIPHERAL BLOOD
  The Lancet, 1989