|
1 Firth HV, Boyd PA, Chamberlain PF, et al. Analysis of limb reduction defects in babies exposed to chorionic villus sampling. Lancet, 1994, 343:1069–1071.
|
|
2 Dennis YM, Rossa LO, Chiu WK. Innovation: Prenatal diagnosis:Progress through plasma nucleic acids. Nature genet Rev, 2007, 8:71–77.
|
|
3 Schmorl G. Pathogisch–anatomische untersuchungen uberpuerperal eklampsie. Leipzig(Germary):Vogel,1893.
|
|
4 Walknoska J, Conte FA, Grumbach MM. Practical and theoretical implications of fetal–maternal lymphocyte transfer. Lancet,1969, (12):1119–1122.
|
|
5 Bianchi DW, Zickwolf GK, Weil GJ, et al. Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum. Proc Acad Sci U S A, 1996, 93(2):705–708.
|
|
6 Saknan M, Sherman E, Dorothy EL, et al. Evaluation of a culture system for enrichment of CD34+ hematopoietic progenitor cells present in maternal blood. Fetal Diagn Ther, 2002, 17:90–96.
|
|
7 Kolialexi A, Tsangaris GT, Antsaklis A, et al. Fetal cells in maternal plasma are found in a late state of apoptosis. Prenat Diagn, 2004, 24:719–721.
|
|
8 Bischoff FZ, Hahn S, Johnson KL, et al. Intact fetal cells in maternal plasma: Are they really there? Lancet, 2003, 361:139–140.
|
|
9 Busch J, Huber P, Holtz J, et al. Simple and fast 'double–MACS' sorting of fetal erythroblasts from maternal blood for PCR–based paternity analysis. Ann NY Acad Sci, 1994, 731:144–146.
|
|
10 Samura O, Sekizawa A, Zhen DK, et al. Comparison of fetal cell recovery from maternal blood using a high density gradient for the initial separation step:1.090 versus 1.119 g/mL. Prenat Diagn, 2000, 20:281–286.
|
|
11 Zhong XY, Hahn S, Steinborn A, et al. Quantitative analysis of intact fetal cells in maternal plasma by real–time PCR. Eur J Obstet Gynecol Reprod Biol, 2006, 133(1):20–24.
|
|
12 Kitagawa M, Sugiura K, Omi H, et al. New technique using galactose–specific lectin for isolation of fetal cells from maternal blood. Prenat Diagn, 2002, 22:17–21.
|
|
13 Purwosunu Y, Sekizawa A, Farina A, et al. Enrichment of NRBC in maternal blood: A more feasible method for noninvasive prenatal diagnosis. Prenat Diagn, 2006, 26:545–547.
|
|
14 Zheng YL, Carter NP, Price CM, et al. Prenatal diagnosis from maternal blood: Simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting. J Med Genet, 1993, 30(12):1051–1056.
|
|
15 Sekizawa A, Purwosunu Y, Matsuoka R, et al. Recent advances in non–invasive prenatal DNA diagnosis through analysis of maternal blood. J Obstet Gynecol Res, 2007, 33(6):747–764.
|
|
16 Borgatti M, Bianchi N, Mancini I, et al. New trends in non–invasive prenatal diagnosis:Applications of dielectrophoresis–based Lab–on–a–chip platforms to the identification and manipulation of rare cells. Int J Mol Med, 2008, 21:3–12.
|
|
17 Cirigliano V, Voglino G, Canadas MP, et al. Rapid prenatal diagnosis of common chromosome aneuploidies by QF–PCR. Assessment on 18 000 consecutive clinical samples. Mol Hum Reprod, 2004, 10(11):839–846.
|
|
18 Krabchi K, Lavoie J, Coullin P, et al. From the conception of the PRINS to its coromation. Med Sci, 2004, 20:465–473.
|