| 1. |
Farideh et al. (2002) Cell-free fetal DNA and intact fetal cells in maternal blood
circulation: implications for first and second trimester non-invasive prenatal diagnosis. Hum. Reprod.
Update 8:493-500
|
| 2. |
Helene et al. (2002) Culture of fetal cells from maternal blood for prenatal diagnosis. Hum.
Reprod. Update 8:523-527
|
| 3. |
Al-Yatama et al. (2001) Detection of Y chromosome-specific DNA in plasma and urine of
pregnant women using nested polymerase chain reaction. Prenat. Diagn. 21:339-402
|
| 4. |
Prieto et al. (2001) Optimization of nucleated red blood cell (NRBC) recovery from
maternal blood collected using both layers of a double density gradient. Prenat Diagn. 21:187-193.
|
| 5. |
Lo D (2000) Fetal DNA in maternal plasma: biology and diagnostic applications. Clin.
Chem. 46:1903-1906.
|
| 6. |
Perl et al. (2000) Detection of male and female fetal DNA in maternal plasma by multiplex
fluorescent polymerase chain reaction amplification of short tandem repeats. Hum. Genet. 106:45-49.
|
| 7. |
Chiesa et al. (1999) Detection of foetal cells in maternal blood and prenatal sex
determination by in situ hybridization. Procedure verification. Genetic Analysis: Biomolecular Engineering
15:41-45.
|
| 8. |
de Alba et al. (1999) Prenatal diagnosis on fetal cells obtained from maternal peripheral
blood: report of 66 cases. Prenat. Diagn. 19:934-940
|
| 9. |
Troeger et al. (1999) Approximately half of the erythroblasts in maternal blood are of
fetal origin. Mol. Hum. Reprod. 5:1162-1165.
|
| 10. |
Ganshirt et al. (1998) Enrichment of fetal nucleated red blood cells from the maternal
circulation for prenatal diagnosis: experiences with triple density gradient and MACS based on more than 600
cases. Fetal Diagn. Ther. 13:276-286.
|
| 11. |
Holzgreve et al. (1998) Prenatal diagnosis using fetal cells enriched from maternal
blood. Croat Med J. 39:115-120.
|
| 12. |
Lo et al. (1998) Quantitative analysis of fetal DNA in maternal plasma and serum:
implications for noninvasive prenatal diagnosis. Am. J. Hum. Genet. 62:768-775.
|
| 13. |
Watanabe et al. (1998) Prenatal diagnosis of ornithine transcarbamylase deficiency by
using a single nucleated erythrocyte from maternal blood. Hum. Genet. 102:611-615
|
| 14. |
Campagnoli et al. (1997) Noninvasive prenatal Diagnosis. Use of density gradient
centrifugation, magnetically activated cell sorting and in situ hybridization. J. Repr. Med. 42:193-199.
|
| 15. |
Bianchi et al. (1996) Male fetus progenitor cells persist on maternal blood for as long as
27 years postpartum. Proc. Natl. Acad. Sci. USA 93:705-708
|
| 16. |
Cheung et al. (1996) Prenatal diagnosis of sickle cells anaemia and thalassaemia by
analysis of fetal cells in maternal blood. Nature Genetics 14:264-268.
|
| 17. |
Sekizawa et al. (1996) Prenatal Diagnosis of Duchenne muscular dystrophy using a single
nucleated erythrocyte in maternal blood. Neurology 46:1350-1353.
|
| 18. |
Busch et al. (1994) Enrichment of fetal cells from maternal blood by high gradient
magnetic cell sorting (double MACS) for PCR-based genetic analysis. Prenat. Dign. 14:1129-1140.
|
| 19. |
Ganshirt-Ahlert et al. (1993) Detection of fetal trisomies 21 and 18 from maternal blood
using triple gradient and magnetic cell sorting. Am. J. Repr. Immun. 30:194-201.
|
| 20. |
Bianchi et al. (1990) Isolation of fetal DNA from nucleated erythrocytes in maternal
blood. Proc. Natl .Acad. Sci. 87:3279-3283.
|
| 21. |
Lo et al. (1990) Detection of single-copy of fetal DNA sequence from maternal blood. Lancet
335:1463-1464
|
