Using fetal cells for prenatal diagnosis: History and recent progress
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[1] D. Ledbetter,et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. , 2012, The New England journal of medicine.
[2] N. Uldbjerg,et al. Fetal Gender and Several Cytokines Are Associated with the Number of Fetal Cells in Maternal Blood – An Observational Study , 2014, PloS one.
[3] S. Sifakis,et al. Microsatellite analysis provides efficient confirmation of fetal trophoblast isolation from maternal circulation , 2001, Prenatal diagnosis.
[4] F. Conte,et al. Practical and theoretical implications of fetal-maternal lymphocyte transfer. , 1969, Lancet.
[5] L. Vissers,et al. Point mutations as a source of de novo genetic disease. , 2013, Current opinion in genetics & development.
[6] F. Lucas,et al. Noninvasive prenatal testing: Impact on genetic counseling, invasive prenatal diagnosis, and trisomy 21 detection , 2014, Journal of clinical ultrasound : JCU.
[7] F. Sipos,et al. Isolation of epsilon‐haemoglobin‐chain positive fetal cells with micromanipulation for prenatal diagnosis , 2005, Prenatal diagnosis.
[8] Bart A Westerman,et al. Circulating trophoblast in maternal blood , 2003, Prenatal diagnosis.
[9] H. C. Fan,et al. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood , 2008, Proceedings of the National Academy of Sciences.
[10] R. Drouin,et al. Evaluation of the impact of density gradient centrifugation on fetal cell loss during enrichment from maternal peripheral blood , 2014, Prenatal diagnosis.
[11] N. Fisk,et al. Characterization of first trimester fetal erythroblasts for non-invasive prenatal diagnosis. , 2003, Molecular human reproduction.
[12] D. Cram,et al. The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities. , 2015, Journal of genetics and genomics = Yi chuan xue bao.
[13] A. Rimm,et al. Transplant or chemotherapy in acute myelogenous leukaemia , 1989 .
[14] K. Klinger,et al. Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data , 2002, Prenatal diagnosis.
[15] P. Stankiewicz,et al. Detection of ≥1 Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays , 2012, Prenatal diagnosis.
[16] A. Borkhardt,et al. A New Workflow for Whole‐Genome Sequencing of Single Human Cells , 2014, Human mutation.
[17] Bernard Lacour,et al. Circulating trophoblastic cells provide genetic diagnosis in 63 fetuses at risk for cystic fibrosis or spinal muscular atrophy. , 2012, Reproductive biomedicine online.
[18] Yan Wang,et al. Quantitative abnormalities of fetal trophoblast cells in maternal circulation in preeclampsia , 2008, Prenatal diagnosis.
[19] C. Cantor,et al. Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma , 2008, Proceedings of the National Academy of Sciences.
[20] N. Uldbjerg,et al. Characterization of Fetal Cells from the Maternal Circulation by Microarray Gene Expression Analysis - Could the Extravillous Trophoblasts Be a Target for Future Cell-Based Non-Invasive Prenatal Diagnosis? , 2013, Fetal Diagnosis and Therapy.
[21] J. Smith,et al. Prenatal diagnosis using fetal cells isolated from maternal peripheral blood: a review. , 1996, Clinical obstetrics and gynecology.
[22] Sijia Lu,et al. Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications. , 2015, Annual review of genomics and human genetics.
[23] Rebecca Yu Zhang,et al. Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing , 2015, Genome research.
[24] T. Lim,et al. Relationship between gestational age and frequency of fetal trophoblasts and nucleated erythrocytes in maternal peripheral blood , 2001, Prenatal Diagnosis.
[25] X. Xie,et al. Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell , 2012, Science.
[26] Jay Shendure,et al. Noninvasive Whole-Genome Sequencing of a Human Fetus , 2012, Science Translational Medicine.
[27] G. Barkai,et al. Trophoblasts Isolated from the Maternal Circulation: In Vitro Expansion and Potential Application in Non-invasive Prenatal Diagnosis , 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[28] Arthur L. Beaudet,et al. Global genetic carrier testing: a vision for the future , 2015, Genome Medicine.
[29] S. Warsof,et al. Uptake of noninvasive prenatal testing at a large academic referral center. , 2014, American journal of obstetrics and gynecology.
[30] Leonore A. Herzenberg,et al. Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[31] C. Oudejans,et al. HLA-G expression in trophoblast cells circulating in maternal peripheral blood during early pregnancy. , 2001, American journal of obstetrics and gynecology.
[32] M. Pisarska,et al. Utilization of noninvasive prenatal testing: impact on referrals for diagnostic testing. , 2015, American journal of obstetrics and gynecology.
[33] G. Weil,et al. Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[34] I. Sargent,et al. Presence of fetal DNA in maternal plasma and serum , 1997, The Lancet.
[35] N. Fisk,et al. Simultaneous fetal cell identification and diagnosis by epsilon-globin chain immunophenotyping and chromosomal fluorescence in situ hybridization. , 2001, Blood.
[36] Jay Shendure,et al. Whole genome prediction for preimplantation genetic diagnosis , 2015, Genome Medicine.