Fetal cells in maternal blood: current and future perspectives.
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W. Holzgreve | S. Hahn | S Hahn | W Holzgreve | R Sant | R. Sant
[1] C. Redman,et al. Cytotrophoblasts: Masters of disguise , 1997, Nature Medicine.
[2] Yun-Ling Zheng,et al. Search for the optimal fetal cell antibody: results of immunophenotyping studies using flow cytometry , 1997, Human Genetics.
[3] Yun-Ling Zheng,et al. Flow sorting of fetal erythroblasts using intracytoplasmic anti‐fetal haemoglobin: Preliminary observations on maternal samples , 1995, Prenatal diagnosis.
[4] K. Nicolaides,et al. Blood transferrin receptor expression in chromosomally abnormal fetuses , 1995, Prenatal diagnosis.
[5] Takeshi Sato,et al. Prenatal Diagnosis of the Fetal RhD Blood Type Using a Single Fetal Nucleated Erythrocyte From Maternal Blood , 1996, Obstetrics and gynecology.
[6] I. Sargent,et al. Isolating and Analyzing Fetal Leukocytes in Maternal Blood a , 1994, Annals of the New York Academy of Sciences.
[7] R. Hubert,et al. Whole genome amplification from a single cell: implications for genetic analysis. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[8] 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.
[9] D. Rubinsztein,et al. Enrichment of fetal nucleated cells from maternal blood: Model test system using cord blood , 1995, Prenatal diagnosis.
[10] Andreas Radbruch,et al. High gradient magnetic cell separation with MACS. , 1990, Cytometry.
[11] P. Jacobs,et al. Practical and theoretical implications of fetal-maternal lymphocyte transfer. , 1969, Lancet.
[12] H. Netten,et al. FISH and chips: automation of fluorescent dot counting in interphase cell nuclei. , 1997, Cytometry.
[13] A. Urquhart,et al. DNA fingerprinting from single cells , 1997, Nature.
[14] S. Latt,et al. Isolation of fetal DNA from nucleated erythrocytes in maternal blood. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[15] W. Holzgreve,et al. Fetal cells in maternal circulation throughout gestation , 1994, The Lancet.
[16] J. Guillet,et al. Solid phase cytometry for detection of rare events. , 1997, Cytometry.
[17] M. Eigen,et al. Sorting single molecules: application to diagnostics and evolutionary biotechnology. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[18] W. Holzgreve,et al. Detection of Fetal Trisomies 21 and 18 From Maternal Blood Using Triple Gradient and Magnetic Cell Sorting , 1993, American journal of reproductive immunology.
[19] Y. Kan,et al. Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood , 1996, Nature Genetics.
[20] K. Fleming,et al. Culture of fetal erythroid cells from maternal peripheral blood , 1994, The Lancet.
[21] D. Rushton. TROPHOBLAST CELLS IN PERIPHERAL BLOOD , 1984, The Lancet.
[22] W. Jones,et al. A MONOCLONAL ANTIBODY TO HUMAN PLACENTAL LACTOGEN HORMONE FACILITATES ISOLATION OF FETAL CELLS FROM MATERNAL BLOOD IN A MODEL SYSTEM , 1996, Prenatal diagnosis.
[23] W. Holzgreve,et al. Magnetic cell sorting and the transferrin receptor as potential means of prenatal diagnosis from maternal blood. , 1992, American journal of obstetrics and gynecology.
[24] A. Pazarbasi,et al. [Prenatal diagnosis]. , 1994, Revista chilena de obstetricia y ginecologia.
[25] A. de la Chapelle,et al. Fetal lymphocytes in the maternal blood. , 1972, Blood.
[26] W. Park,et al. EMBOLISM TO THE LUNGS BY TROPHOBLAST , 1961, The Journal of obstetrics and gynaecology of the British Commonwealth.
[27] D. Furst,et al. Microchimerism and HLA-compatible relationships of pregnancy in scleroderma , 1998, The Lancet.
[28] P. Matzinger,et al. The maternal immune system's interaction with circulating fetal cells. , 1997, Journal of immunology.
[29] H. Takabayashi,et al. Development of non‐invasive fetal DNA diagnosis from maternal blood , 1995, Prenatal diagnosis.
[30] J. Goldberg. Fetal cells in maternal circulation: progress in analysis of a rare event. , 1997, American journal of human genetics.
[31] T. Hsieh,et al. Presence of Cells of Fetal Origin in Maternal Circulation of Pregnant Women , 1994, Annals of the New York Academy of Sciences.
[32] T. Arinami,et al. Mid‐trimester fetal sex determination from maternal peripheral blood by fluorescence in situ hybridization without enrichment of fetal cells , 1995, Prenatal diagnosis.
[33] K. Klinger,et al. Prenatal diagnosis by use of fetal cells isolated from maternal blood. , 1995, American journal of obstetrics and gynecology.
[34] F. Bischoff,et al. Isolating fetal nucleated red blood cells from maternal blood: The baylor experience—1995 , 1995, Prenatal diagnosis.
[35] W. Holzgreve,et al. Detection of fetal DNA in maternal blood by PCR , 1990, The Lancet.
[36] H. Nakauchi,et al. The Proportion of Fetal Nucleated Red Blood Cells in Maternal Blood: Stimation by FACS Analysis , 1997, Prenatal diagnosis.
[37] F. E. Whitacre,et al. Fetal Erythrocytes in the Maternal Circulation of Pregnant Women , 1964, Obstetrics and gynecology.
[38] W. Holzgreve. Will ultrasound‐screening and ultrasound‐guided procedures be replaced by non‐invasive techniques for the diagnosis of fetal chromosome anomalies? , 1997, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.
[39] 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.
[40] I. Mackenzie,et al. Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers , 1993, The Lancet.
[41] S. Wachtel,et al. Fetal cells in maternal blood: recovery by charge flow separation , 1996, Human Genetics.
[42] J. Goldberg,et al. Incidence and outcome of chromosomal mosaicism found at the time of chorionic villus sampling. , 1997, American journal of obstetrics and gynecology.
[43] I. Sargent,et al. Presence of fetal DNA in maternal plasma and serum , 1997, The Lancet.
[44] E. Graf,et al. Prenatal Diagnosis of Fetal Lymphocytes in the Maternal Blood , 1972, Obstetrics and gynecology.
[45] S. Latt,et al. Analysis of peripheral maternal blood samples for the presence of placenta‐derived cells using Y‐specific probes and McAb H315 , 1988, Prenatal diagnosis.
[46] K. Fleming,et al. PRENATAL SEX DETERMINATION BY DNA AMPLIFICATION FROM MATERNAL PERIPHERAL BLOOD , 1989, The Lancet.
[47] N. Carter,et al. Simultaneous Immunophenotyping and FISH on Fetal Cells from Maternal Blood a , 1994, Annals of the New York Academy of Sciences.
[48] W. Holzgreve,et al. Noninvasive Prenatal Diagnosis Strategy for a Clinical Trial , 1994, Annals of the New York Academy of Sciences.
[49] D. Valerio,et al. Culture of fetal erythroid progenitor cells from maternal blood for non-invasive prenatal genetic diagnosis. , 1997, Prenatal Diagnosis.
[50] W. Holzgreve,et al. Successful Prenatal Diagnosis from Maternal Blood with Magnetic‐Activated Cell Sorting , 1994, Annals of the New York Academy of Sciences.
[51] N. Odartchenko,et al. [Post-partum survival of fetal lymphocytes in the maternal blood]. , 1977, Schweizerische medizinische Wochenschrift.
[52] K. Klinger,et al. Maternal origin of transferrin receptor positive cells in venous blood of pregnant women , 1996, Clinical genetics.
[53] H. von Koskull,et al. Fetal erythroblasts from maternal blood identified with 2,3‐bisphosphoglycerate (BPG) and in situ hybridization (ISH) using Y‐specific probes , 1995, Prenatal diagnosis.
[54] L. Grosset,et al. ANTENATAL FETAL SEX DETERMINATION FROM MATERNAL BLOOD DURING EARLY PREGNANCY , 1975 .
[55] E. Ascari,et al. Characterization of the biophysical properties of human erythroblasts as a preliminary step to the isolation of fetal erythroblasts from maternal peripheral blood for non invasive prenatal genetic investigation. , 1997, Haematologica.
[56] I. Sargent,et al. Clinical Experience: Isolating Trophoblasts from Maternal Blood a , 1994, Annals of the New York Academy of Sciences.
[57] W. Holzgreve,et al. Ratio of fetal to maternal DNA is less than 1 in 5000 at different gestational ages in maternal blood , 1990, Clinical genetics.
[58] C. Camaschella,et al. Circulating ‘trophoblast’ cells in pregnancy have maternal genetic markers , 1988, Prenatal diagnosis.
[59] U. Claussen,et al. Determination of the origin of single nucleated cells in maternal circulation by means of random PCR and a set of length polymorphisms , 1997, Human Genetics.
[60] D. Valerio,et al. Isolation of fetal erythroid cells from maternal blood based on expression of erythropoietin receptors. , 1997, Molecular human reproduction.
[61] M. Sasaki,et al. Prenatal diagnosis of Duchenne muscular dystrophy using a single fetal nucleated erythrocyte in maternal blood , 1996, Neurology.
[62] F. Bischoff,et al. Rare event selection of fetal nucleated erythrocytes in maternal blood by flow cytometry. , 1996, Cytometry.
[63] W. Holzgreve,et al. Fetal cells in the maternal circulation. , 1992, The Journal of reproductive medicine.
[64] Z. Rudzki,et al. Detection of Paternally Inherited Mutations for β‐Thalassemia in Trophoblast Isolated from Peripheral Maternal Blood a , 1994, Annals of the New York Academy of Sciences.
[65] J. Delhanty,et al. Preimplantation genetic diagnosis: strategies and surprises. , 1997, Trends in genetics : TIG.
[66] J. Smith,et al. Prenatal diagnosis using fetal cells isolated from maternal peripheral blood: a review. , 1996, Clinical obstetrics and gynecology.
[67] D. Bianchi,et al. DEVELOPMENT OF A MODEL SYSTEM TO COMPARE CELL SEPARATION METHODS FOR THE ISOLATION OF FETAL CELLS FROM MATERNAL BLOOD , 1996, Prenatal diagnosis.
[68] D. Bianchi,et al. Erythroid‐specific antibodies enhance detection of fetal nucleated erythrocytes in maternal blood , 1993, Prenatal diagnosis.
[69] C. Oudejans,et al. Identification of hash2-positive extravillus trophoblast cells in the peripheral blood of pregnant women , 1998 .
[70] N. Carter,et al. Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting. , 1993, Journal of medical genetics.