Investigation of maternal blood enriched for fetal cells: Role in screening and diagnosis of fetal trisomies
- 20 May 1999
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Prenatal diagnosis of trisomy 18 at the 10–14‐week ultrasound scanUltrasound in Obstetrics & Gynecology, 1997
- Increased Nuchal Translucency as a Marker for Fetal Chromosomal DefectsNew England Journal of Medicine, 1997
- Isolating fetal nucleated red blood cells from maternal blood: The baylor experience—1995Prenatal Diagnosis, 1995
- Maternal Age and Gestational Age-Specific Risk for Chromosomal DefectsFetal Diagnosis and Therapy, 1995
- Isolating fetal cells in maternal circulation for prenatal diagnosisPrenatal Diagnosis, 1994
- Detection of Fetal Trisomies 21 and 18 From Maternal Blood Using Triple Gradient and Magnetic Cell SortingAmerican Journal of Reproductive Immunology, 1993
- Fetal nucleated cells in maternal peripheral blood: frequency and relationship to gestational ageHuman Genetics, 1993
- Detection of fetal cells with 47,XY,+21 karyotype in maternal peripheral bloodHuman Genetics, 1992
- Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy.BMJ, 1992
- PRACTICAL AND THEORETICAL IMPLICATIONS OF FETAL/MATERNAL LYMPHOCYTE TRANSFERThe Lancet, 1969