Prenatal diagnosis by use of fetal cells isolated from maternal blood

American Journal of Obstetrics and Gynecology

Volumn 173, Issue 4, 1995, Pages 1354-1355

  de la Cruz, Felix ^a   Shifrin, Harvey ^a   Elias, Sherman ^b   Simpson, Joe Leigh ^b   Jackson, Laird ^c   Klinger, Katherine ^d   Bianchi, Diana W ^e   Kaplan, Sherrie H ^e   Evans, Mark I ^f   Holzgreve, Wolfgang ^g   Gänshirt, Dorothee ^g  

^a Building 6100 Suite 4B09 6100 Executive Blvd MSC 7510 Bethesda MD 20892 7510 USA ^*

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c THOMAS JEFFERSON UNIVERSITY   (United States)

^d Integrated Genetics   (United States)

^e TUFTS MEDICAL CENTER   (United States)

^f WAYNE STATE UNIVERSITY   (United States)

^g UNIVERSITY WOMEN S HOSPITAL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; CELL ISOLATION; CHROMOSOME ABERRATION; CYTOGENETICS; FETUS CELL; HUMAN; LETTER; MATERNAL BLOOD; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

CELL SEPARATION; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; FETAL DISEASES; FETUS; HUMAN; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0028863599     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/0002-9378(95)91393-9     Document Type: Letter

References (5)

1. Prenatal diagnosis using fetal cells isolated from maternal blood by multiparameter flow cytometry
2. Detection of fetal cells with 47,XY, + 21 karyotype in maternal peripheral blood
3. First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood
4. Detection of Fetal Trisomies 21 and 18 From Maternal Blood Using Triple Gradient and Magnetic Cell Sorting
5. Isolation of fetal DNA from nucleated erythrocytes in maternal blood