Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.
暂无分享,去创建一个
T K Lau | N M Hjelm | Y. Lo | N. M. Hjelm | M. Tein | P. Johnson | T. Lau | T. Leung | P J Johnson | P M Poon | C. Haines | C J Haines | T N Leung | J. Wainscoat | J. S. Wainscoat | Y M Lo | J S Wainscoat | P. Poon | A. Chang | M S Tein | A M Chang | Allan M Chang | P. Johnson | Tze K. Lau | Y. D. Lo | Allan M. Z. Chang | Christopher J. Haines | Priscilla M.K. Poon | Philip J. Johnson | N. M. Hjelm
[1] H. Nakauchi,et al. The Proportion of Fetal Nucleated Red Blood Cells in Maternal Blood: Stimation by FACS Analysis , 1997, Prenatal diagnosis.
[2] K. Fleming,et al. PRENATAL SEX DETERMINATION BY DNA AMPLIFICATION FROM MATERNAL PERIPHERAL BLOOD , 1989, The Lancet.
[3] John A. Todd,et al. Towards fully automated genome–wide polymorphism screening , 1995, Nature Genetics.
[4] V. Vasioukhin,et al. K-ras mutations are found in DNA extracted from the plasma of patients with colorectal cancer. , 1997, Gastroenterology.
[5] 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.
[6] K. Klinger,et al. Fetal cells in maternal blood: determination of purity and yield by quantitative polymerase chain reaction. , 1994, American journal of obstetrics and gynecology.
[7] R. Abramson,et al. Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[8] I. Sargent,et al. Presence of fetal DNA in maternal plasma and serum , 1997, The Lancet.
[9] Y. Kan,et al. Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood , 1996, Nature Genetics.
[10] I. Sargent,et al. Two-way cell traffic between mother and fetus: biologic and clinical implications. , 1996, Blood.
[11] Boland Cr. Setting microsatellites free. , 1996 .
[12] David Sidransky,et al. Microsatellite alterations in serum DNA of head and neck cancer patients , 1996, Nature Medicine.
[13] J. Hartley,et al. Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reactions. , 1990, Gene.
[14] F. Conte,et al. Practical and theoretical implications of fetal-maternal lymphocyte transfer. , 1969, Lancet.
[15] 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.
[16] A. Rimm,et al. Transplant or chemotherapy in acute myelogenous leukaemia , 1989 .
[17] S. Kwok,et al. Avoiding false positives with PCR , 1989, Nature.
[18] A. Kurt,et al. Microsatellite alterations in plasma DNA of small cell lung cancer patients , 1996, Nature Medicine.
[19] I. Mackenzie,et al. Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers , 1993, The Lancet.
[20] C. R. Connell,et al. Allelic discrimination by nick-translation PCR with fluorogenic probes. , 1993, Nucleic acids research.
[21] M. Sharf,et al. Fetal obstructive uropathy [corrected]. , 1988, Lancet.
[22] K. Livak,et al. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. , 1995, PCR methods and applications.
[23] K. Klinger,et al. PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies. , 1997, American journal of human genetics.
[24] Y. Lo,et al. Strategies for the Detection of Autosomal Fetal DNA Sequence from Maternal Peripheral Blood , 1994, Annals of the New York Academy of Sciences.
[25] G. Saglio,et al. Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood. , 1990, Blood.
[26] J. Simpson,et al. Isolating fetal cells from maternal blood. Advances in prenatal diagnosis through molecular technology. , 1993, JAMA.