{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,23]],"date-time":"2023-09-23T19:58:57Z","timestamp":1695499137535},"reference-count":47,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2010,9,1]],"date-time":"2010-09-01T00:00:00Z","timestamp":1283299200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinics in Laboratory Medicine"],"published-print":{"date-parts":[[2010,9]]},"DOI":"10.1016\/j.cll.2010.04.011","type":"journal-article","created":{"date-parts":[[2010,7,17]],"date-time":"2010-07-17T08:54:09Z","timestamp":1279356849000},"page":"655-665","source":"Crossref","is-referenced-by-count":9,"title":["Noninvasive Prenatal Diagnosis: 2010"],"prefix":"10.1016","volume":"30","author":[{"given":"Mark I.","family":"Evans","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael","family":"Kilpatrick","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.cll.2010.04.011_bib1","series-title":"Prenatal diagnosis: genetics, reproductive risks, testing, and management","year":"2006"},{"issue":"4","key":"10.1016\/j.cll.2010.04.011_bib2","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1053\/j.semperi.2005.06.004","article-title":"Invasive prenatal diagnostic procedures 2005","volume":"29","author":"Evans","year":"2005","journal-title":"Semin Perinatol"},{"key":"10.1016\/j.cll.2010.04.011_bib3","series-title":"Clinical obstetrics and gynecology \u2013 new genetics for the clinician","first-page":"657","article-title":"Principles of screening","author":"Evans","year":"2002"},{"key":"10.1016\/j.cll.2010.04.011_bib4","unstructured":"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."},{"key":"10.1016\/j.cll.2010.04.011_bib5","doi-asserted-by":"crossref","first-page":"609","DOI":"10.1002\/pd.347","article-title":"Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I Data","volume":"22","author":"Bianchi","year":"2002","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib6","doi-asserted-by":"crossref","first-page":"1453","DOI":"10.1073\/pnas.76.3.1453","article-title":"Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting","volume":"76","author":"Herzenberg","year":"1979","journal-title":"Proc Natl Acad Sci U\u00a0S\u00a0A"},{"key":"10.1016\/j.cll.2010.04.011_bib7","series-title":"Fetal cells and fetal DNA in maternal blood: new developments for a new millennium","year":"2001"},{"key":"10.1016\/j.cll.2010.04.011_bib8","series-title":"Fetal cells and fetal DNA in maternal blood: new developments for a new millennium","first-page":"28","article-title":"Fetal cells in maternal blood: an overview of the basel experience","author":"Holzgreve","year":"2001"},{"key":"10.1016\/j.cll.2010.04.011_bib9","doi-asserted-by":"crossref","first-page":"218","DOI":"10.1086\/302205","article-title":"Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis","volume":"64","author":"Lo","year":"1999","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.cll.2010.04.011_bib10","doi-asserted-by":"crossref","first-page":"218","DOI":"10.1038\/nm1530","article-title":"Development of extraction protocols to improve the yield for fetal RNA in maternal plasma","volume":"13","author":"Lo","year":"2007","journal-title":"Nat Med"},{"key":"10.1016\/j.cll.2010.04.011_bib11","doi-asserted-by":"crossref","first-page":"164","DOI":"10.1097\/AOG.0b013e31817d453c","article-title":"Management of Rhesus alloimmunization in pregnancy","volume":"112","author":"Moise","year":"2008","journal-title":"Obstet Gynecol"},{"key":"10.1016\/j.cll.2010.04.011_bib12","series-title":"High risk obstetrics in the requisites in obstetrics and gynecology","first-page":"33","article-title":"Genetic screening and clinical testing","author":"Evans","year":"2008"},{"key":"10.1016\/j.cll.2010.04.011_bib13","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1016\/S0140-6736(03)12191-5","article-title":"Intact fetal cells in maternal plasma: are they really there?","volume":"361","author":"Bischoff","year":"2003","journal-title":"Lancet"},{"key":"10.1016\/j.cll.2010.04.011_bib14","doi-asserted-by":"crossref","first-page":"1571","DOI":"10.1016\/j.ajog.2004.03.055","article-title":"Getting fetal cells in maternal blood to work: eliminating the false positive XY signals in XX pregnancies","volume":"190","author":"Kilpatrick","year":"2004","journal-title":"Am J Obstet Gynecol"},{"issue":"9","key":"10.1016\/j.cll.2010.04.011_bib15","doi-asserted-by":"crossref","first-page":"815","DOI":"10.1002\/pd.1987","article-title":"Detection of circulating fetal cells utilizing automated microscopy: potential for noninvasive prenatal diagnosis of chromosomal aneuploidies","volume":"28","author":"Seppo","year":"2008","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib16","doi-asserted-by":"crossref","first-page":"892","DOI":"10.1002\/pd.2079","article-title":"A\u00a0microfluidics approach for the solation of nucleated red blood cells (NRBCs) from peripheral blood of pregnant women","volume":"28","author":"Huang","year":"2008","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib17","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1369\/jhc.4B6421.2005","article-title":"New aspects of laser microdissection in research and routine","volume":"53","author":"Burgemeister","year":"2005","journal-title":"J\u00a0Histochem Cytochem"},{"key":"10.1016\/j.cll.2010.04.011_bib18","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1093\/humupd\/3.4.383","article-title":"First trimester prenatal diagnosis using transcervical cells: an evaluation","volume":"3","author":"Adinolfi","year":"1997","journal-title":"Hum Reprod Update"},{"key":"10.1016\/j.cll.2010.04.011_bib19","doi-asserted-by":"crossref","first-page":"619","DOI":"10.1002\/pd.117","article-title":"Fetal cells in the uterine cervix: a source for early non-invasive prenatal diagnosis","volume":"21","author":"Fejgin","year":"2001","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib20","doi-asserted-by":"crossref","first-page":"1098","DOI":"10.1002\/pd.469","article-title":"Strategies for the isolation and detection of fetal cells in transcervical samples","volume":"22","author":"Bussani","year":"2002","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib21","doi-asserted-by":"crossref","first-page":"198","DOI":"10.1002\/pd.1104","article-title":"Comparison of two techniques for transcervical cell sampling performed in the same study population","volume":"25","author":"Cioni","year":"2005","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib22","doi-asserted-by":"crossref","first-page":"933","DOI":"10.1002\/pd.1970151008","article-title":"Methods for the transcervical collection of fetal cells during the first trimester of pregnancy","volume":"15","author":"Rodeck","year":"1995","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib23","doi-asserted-by":"crossref","first-page":"150","DOI":"10.1007\/BF02265257","article-title":"Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells","volume":"97","author":"Massari","year":"1996","journal-title":"Hum Genet"},{"key":"10.1016\/j.cll.2010.04.011_bib24","doi-asserted-by":"crossref","first-page":"595","DOI":"10.1111\/j.1471-0528.2004.00506.x","article-title":"DNA identification of fetal cells isolated from cervical mucus: potential for early non-invasive prenatal diagnosis","volume":"112","author":"Katz-Jaffe","year":"2005","journal-title":"BJOG"},{"key":"10.1016\/j.cll.2010.04.011_bib25","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1016\/S0140-6736(97)02174-0","article-title":"Presence of fetal DNA in maternal plasma and serum","volume":"350","author":"Lo","year":"1997","journal-title":"Lancet"},{"key":"10.1016\/j.cll.2010.04.011_bib26","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1373\/clinchem.2003.024893","article-title":"Size distributions of maternal and fetal DNA in maternal plasma","volume":"50","author":"Chan","year":"2004","journal-title":"Clin Chem"},{"key":"10.1016\/j.cll.2010.04.011_bib27","doi-asserted-by":"crossref","first-page":"843","DOI":"10.1001\/jama.293.7.843","article-title":"Detection of paternally inherited fetal point mutations for beta-thalassemia using size fractionated cell free DNA in maternal plasma","volume":"293","author":"Li","year":"2005","journal-title":"JAMA"},{"key":"10.1016\/j.cll.2010.04.011_bib28","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1093\/clinchem\/48.1.35","article-title":"Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma","volume":"48","author":"Poon","year":"2002","journal-title":"Clin Chem"},{"key":"10.1016\/j.cll.2010.04.011_bib29","first-page":"35","article-title":"Detection of the placental epigenetic signature of the maspin gene in maternal plasma","volume":"48","author":"Chim","year":"2002","journal-title":"Clin Chem"},{"key":"10.1016\/j.cll.2010.04.011_bib30","doi-asserted-by":"crossref","first-page":"152","DOI":"10.1111\/j.1471-0528.2008.02010.x","article-title":"Non invasive prenatal detection of fetal chromosomal aneuploidies by maternal plasma nucleic acid analysis: a review of the current state of the art","volume":"116","author":"Lo","year":"2009","journal-title":"Br J Obstet Gynaecol"},{"key":"10.1016\/j.cll.2010.04.011_bib32","doi-asserted-by":"crossref","first-page":"13116","DOI":"10.1073\/pnas.0705765104","article-title":"Digital PCR for the molecular detection of fetal chromosomal aneuploidy","volume":"104","author":"Lo","year":"2007","journal-title":"Proc Natl Acad Sci U\u00a0S\u00a0A"},{"key":"10.1016\/j.cll.2010.04.011_bib33","doi-asserted-by":"crossref","first-page":"543","DOI":"10.1016\/j.ajog.2009.03.002","article-title":"Microfluidic digital PCR enables rapid prenatal diagnosis of fetal aneuploidy","volume":"200","author":"Fan","year":"2009","journal-title":"Am J Obstet Gynecol"},{"key":"10.1016\/j.cll.2010.04.011_bib34","doi-asserted-by":"crossref","first-page":"9236","DOI":"10.1073\/pnas.96.16.9236","article-title":"Digital PCR","volume":"96","author":"Vogelstein","year":"1999","journal-title":"Proc Natl Acad Sci U\u00a0S\u00a0A"},{"key":"10.1016\/j.cll.2010.04.011_bib35","doi-asserted-by":"crossref","first-page":"613","DOI":"10.1586\/erm.09.43","article-title":"Noninvasive prenatal diagnosis of fetal aneuploidies and Mendelian disorders: new innovative strategies","volume":"9","author":"Hahn","year":"2009","journal-title":"Expert Rev Mol Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib36","doi-asserted-by":"crossref","first-page":"16266","DOI":"10.1073\/pnas.0808319105","article-title":"Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood","volume":"105","author":"Fan","year":"2008","journal-title":"Proc Natl Acad Sci U\u00a0S\u00a0A"},{"key":"10.1016\/j.cll.2010.04.011_bib37","doi-asserted-by":"crossref","first-page":"20458","DOI":"10.1073\/pnas.0810641105","article-title":"Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma","volume":"105","author":"Chiu","year":"2008","journal-title":"Proc Natl Acad Sci U\u00a0S\u00a0A"},{"key":"10.1016\/j.cll.2010.04.011_bib38","doi-asserted-by":"crossref","first-page":"1163","DOI":"10.1016\/j.ajog.2006.07.033","article-title":"Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood \u2013 a meta analysis","volume":"195","author":"Geifman-Holtzman","year":"2006","journal-title":"Am J Obstet Gynecol"},{"key":"10.1016\/j.cll.2010.04.011_bib39","doi-asserted-by":"crossref","first-page":"S173","DOI":"10.1016\/j.ajog.2007.10.629","article-title":"Non-invasive prenatal testing: technical strategies to achieve testing of cell free fetal DNA RhD genotype in a clinical lab","volume":"197","author":"Brown","year":"2007","journal-title":"Am J Obstet Gynecol"},{"key":"10.1016\/j.cll.2010.04.011_bib40","doi-asserted-by":"crossref","first-page":"998","DOI":"10.1016\/S0140-6736(02)11086-5","article-title":"Prenatal exclusion of beta thalassaemia major by examination of maternal plasma","volume":"360","author":"Chiu","year":"2002","journal-title":"Lancet"},{"key":"10.1016\/j.cll.2010.04.011_bib41","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1002\/pd.1608","article-title":"Non-invasive prenatal detection of achondroplasia in size fractionated cell-free DNA by MALDI-TOF MS assay","volume":"27","author":"Li","year":"2007","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.cll.2010.04.011_bib42","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1097\/AOG.0b013e3181c3c938","article-title":"Reliability of fetal sex determination using maternal plasma","volume":"115","author":"Scheffer","year":"2010","journal-title":"Obstet Gynecol"},{"key":"10.1016\/j.cll.2010.04.011_bib43","doi-asserted-by":"crossref","first-page":"140","DOI":"10.1159\/000069366","article-title":"Demographic factors for utilization of invasive genetic testing after multifetal pregnancy reduction (MFPR)","volume":"18","author":"Baker","year":"2003","journal-title":"Fetal Diagn Ther"},{"key":"10.1016\/j.cll.2010.04.011_bib44","series-title":"A\u00a0practical guide to fetal echocardiography","author":"Abuhamad","year":"2010"},{"key":"10.1016\/j.cll.2010.04.011_bib45","doi-asserted-by":"crossref","first-page":"2001","DOI":"10.1056\/NEJMoa043693","article-title":"First trimester or second trimester screening or both for Down's Syndrome","volume":"353","author":"Malone","year":"2005","journal-title":"N\u00a0Engl J Med"},{"key":"10.1016\/j.cll.2010.04.011_bib46","doi-asserted-by":"crossref","first-page":"308","DOI":"10.1159\/000123619","article-title":"Screening advances and diagnostic choice: the problem of residual risk","volume":"23","author":"Henry","year":"2008","journal-title":"Fetal Diagn Ther"},{"key":"10.1016\/j.cll.2010.04.011_bib47","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1159\/000291490","article-title":"Impact of quality of nuchal translucency measurements on detection rates of Trisomies 13 and 18","volume":"27","author":"Evans","year":"2010","journal-title":"Fetal Diagn Ther"},{"key":"10.1016\/j.cll.2010.04.011_bib48","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1097\/00125817-200107000-00006","article-title":"Favorable attitudes toward testing for chromosomal abnormalities via analysis of fetal cells in maternal blood","volume":"4","author":"Zamerowski","year":"2001","journal-title":"Genet Med"}],"container-title":["Clinics in Laboratory Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0272271210000430?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0272271210000430?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,6,7]],"date-time":"2020-06-07T04:24:30Z","timestamp":1591503870000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0272271210000430"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,9]]},"references-count":47,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2010,9]]}},"alternative-id":["S0272271210000430"],"URL":"https:\/\/doi.org\/10.1016\/j.cll.2010.04.011","relation":{},"ISSN":["0272-2712"],"issn-type":[{"value":"0272-2712","type":"print"}],"subject":[],"published":{"date-parts":[[2010,9]]}}}