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- Evans M.I. Johnson M.P. Yaron Y. Prenatal diagnosis: genetics, reproductive risks, testing, and management. McGraw Hill Publishing Co, New York2006
- Invasive prenatal diagnostic procedures 2005.Semin Perinatol. 2005; 29: 215-218
- Principles of screening.in: Evans M.I. Clinical obstetrics and gynecology – new genetics for the clinician. Lippincott, Williams & Wilkins, Philadelphia2002: 657-660
Evans MI, Andriole S. Screening and testing in multiples. In: Odibo A, Krantz DA, editors. Prenatal screening and diagnosis clinics in laboratory medicine. Philadelphia: Elsevier Saunders Publishing C, in press.
- Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I Data.Prenat Diagn. 2002; 22: 609-615
- Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting.Proc Natl Acad Sci U S A. 1979; 76: 1453-1455
- Hahn S. Holzgreve W. Fetal cells and fetal DNA in maternal blood: new developments for a new millennium. Karger Publishing Co, Basel (Switzerland)2001
- Fetal cells in maternal blood: an overview of the basel experience.in: Hahn S. Holzgreve W. Fetal cells and fetal DNA in maternal blood: new developments for a new millennium. Karger Publishing Co, Basel (Switzerland)2001: 28-36
- Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.Am J Hum Genet. 1999; 64: 218-224
- Development of extraction protocols to improve the yield for fetal RNA in maternal plasma.Nat Med. 2007; 13: 218-223
- Management of Rhesus alloimmunization in pregnancy.Obstet Gynecol. 2008; 112: 164-176
- Genetic screening and clinical testing.in: Funai E. Evans M.I. Lockwood J. High risk obstetrics in the requisites in obstetrics and gynecology. Elsevier Science, Philadelphia2008: 33-60
- Intact fetal cells in maternal plasma: are they really there?.Lancet. 2003; 361: 139-140
- Getting fetal cells in maternal blood to work: eliminating the false positive XY signals in XX pregnancies.Am J Obstet Gynecol. 2004; 190: 1571-1581
- Detection of circulating fetal cells utilizing automated microscopy: potential for noninvasive prenatal diagnosis of chromosomal aneuploidies.Prenat Diagn. 2008; 28: 815-821
- A microfluidics approach for the solation of nucleated red blood cells (NRBCs) from peripheral blood of pregnant women.Prenat Diagn. 2008; 28: 892-899
- New aspects of laser microdissection in research and routine.J Histochem Cytochem. 2005; 53: 409-412
- First trimester prenatal diagnosis using transcervical cells: an evaluation.Hum Reprod Update. 1997; 3: 383-392
- Fetal cells in the uterine cervix: a source for early non-invasive prenatal diagnosis.Prenat Diagn. 2001; 21: 619-621
- Strategies for the isolation and detection of fetal cells in transcervical samples.Prenat Diagn. 2002; 22: 1098-1101
- Comparison of two techniques for transcervical cell sampling performed in the same study population.Prenat Diagn. 2005; 25: 198-202
- Methods for the transcervical collection of fetal cells during the first trimester of pregnancy.Prenat Diagn. 1995; 15: 933-942
- Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells.Hum Genet. 1996; 97: 150-155
- DNA identification of fetal cells isolated from cervical mucus: potential for early non-invasive prenatal diagnosis.BJOG. 2005; 112: 595-600
- Presence of fetal DNA in maternal plasma and serum.Lancet. 1997; 350: 485-487
- Size distributions of maternal and fetal DNA in maternal plasma.Clin Chem. 2004; 50: 88-92
- Detection of paternally inherited fetal point mutations for beta-thalassemia using size fractionated cell free DNA in maternal plasma.JAMA. 2005; 293: 843-849
- Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma.Clin Chem. 2002; 48: 35-41
- Detection of the placental epigenetic signature of the maspin gene in maternal plasma.Clin Chem. 2002; 48: 35-41
- Non invasive prenatal detection of fetal chromosomal aneuploidies by maternal plasma nucleic acid analysis: a review of the current state of the art.Br J Obstet Gynaecol. 2009; 116: 152-157
- (Available at:) (Accessed June 1, 2010)
- Digital PCR for the molecular detection of fetal chromosomal aneuploidy.Proc Natl Acad Sci U S A. 2007; 104: 13116-13121
- Microfluidic digital PCR enables rapid prenatal diagnosis of fetal aneuploidy.Am J Obstet Gynecol. 2009; 200 (e1–543.e7): 543
- Digital PCR.Proc Natl Acad Sci U S A. 1999; 96: 9236-9241
- Noninvasive prenatal diagnosis of fetal aneuploidies and Mendelian disorders: new innovative strategies.Expert Rev Mol Diagn. 2009; 9: 613-621
- Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood.Proc Natl Acad Sci U S A. 2008; 105: 16266-16271
- Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.Proc Natl Acad Sci U S A. 2008; 105: 20458-20463
- Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood – a meta analysis.Am J Obstet Gynecol. 2006; 195: 1163-1173
- Non-invasive prenatal testing: technical strategies to achieve testing of cell free fetal DNA RhD genotype in a clinical lab.Am J Obstet Gynecol. 2007; 197: S173
- Prenatal exclusion of beta thalassaemia major by examination of maternal plasma.Lancet. 2002; 360: 998-1000
- Non-invasive prenatal detection of achondroplasia in size fractionated cell-free DNA by MALDI-TOF MS assay.Prenat Diagn. 2007; 27: 11-17
- Reliability of fetal sex determination using maternal plasma.Obstet Gynecol. 2010; 115: 117-126
- Demographic factors for utilization of invasive genetic testing after multifetal pregnancy reduction (MFPR).Fetal Diagn Ther. 2003; 18: 140-143
- A practical guide to fetal echocardiography.2nd edition. Wolters Kluwer/Lippincott, Philadelphia2010
- First trimester or second trimester screening or both for Down's Syndrome.N Engl J Med. 2005; 353: 2001-2011
- Screening advances and diagnostic choice: the problem of residual risk.Fetal Diagn Ther. 2008; 23: 308-315
- Impact of quality of nuchal translucency measurements on detection rates of Trisomies 13 and 18.Fetal Diagn Ther. 2010; 27: 68-71
- Favorable attitudes toward testing for chromosomal abnormalities via analysis of fetal cells in maternal blood.Genet Med. 2001; 4: 301-309