共 16 条
[1]
Bianchi D.W., Stewart J.E., Garber M.F., Lucotte G., Flint A.F., Possible effect of gestational age on the detection of fetal nucleated erythrocytes in maternal blood, Prenat Diagn, 11, pp. 523-528, (1991)
[2]
Bianchi D.W., Yih M.C., Zickwolf G.K., Flint A.F., Transferrin receptor (CD71) expression on circulating mononuclear cells during pregnancy, Am J Obstet Gynecol, 170, pp. 202-206, (1994)
[3]
Bianchi D.W., Shuber A.P., DeMaria M.A., Fougner A.C., Klinger K.W., Fetal cells in maternal blood: Determination of purity and yield by quantitative polymerase chain reaction, Am J Obstet Gynecol, 171, pp. 922-926, (1994)
[4]
Busch J., Huber P., Pfluger E., Miltenyi S.T., Holtz J., Radbruch A., Enrichment of fetal cells from maternal blood by high gradient magnetic cell sorting (double MACS) for PCR-based genetic analysis, Prenatal Diagnosis, 14, pp. 1129-1140, (1994)
[5]
Daffos F., Forestier F., Fetal hematology, Medicine of the fetus & mother, pp. 173-180, (1992)
[6]
Ganshirt-Ahlert D., Burschyk M., Garritsen H.S.P., Helmer L., Miny P., Horst J., Schneider H.P.G., Holzgreve W., Magnetic cell sorting and the transferrin receptor as potential means of prenatal diagnosis from maternal blood, American Journal of Obstetrics and Gynecology, 166, pp. 1350-1355, (1992)
[7]
Ganshirt-Ahlert D., Borjesson-Stoll R., Burschyk M., Dohr A., Garritsen H.S.P., Helmer E., Miny P., Velasco M., Walde C., Patterson D., Teng N., Bhat N.M., Bieber M.M., Holzgreve W., Detection of fetal trisomies 21 and 18 from maternal blood using triple gradient and magnetic cell sorting, American Journal of Reproductive Immunology, 30, pp. 194-201, (1993)
[8]
Howells, Jones S.E., Napier J.A.F., Saunders K., Cavill I., Erythropoiesis in pregnancy, Br J Haematol, 64, pp. 595-599, (1986)
[9]
Knuutila S., Nylund S.J., Wessman M., Larramendy M.L., Analysis of genotype and phenotype on the same interphase or mitotic cell. A manual of MAC (morphology antibody chromosomes) methodology, Cancer Genet Cytogenet, 72, pp. 1-15, (1994)
[10]
Kogan S.C., Doherty M., Gitschier J., An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences, New Engl J Med, 317, pp. 985-990, (1987)