{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,1]],"date-time":"2022-04-01T12:29:59Z","timestamp":1648816199702},"reference-count":20,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2017,1,1]],"date-time":"2017-01-01T00:00:00Z","timestamp":1483228800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Gyn\u00e9cologie Obst\u00e9trique Fertilit\u00e9 & S\u00e9nologie\u00a0"],"published-print":{"date-parts":[[2017,1]]},"DOI":"10.1016\/j.gofs.2016.12.014","type":"journal-article","created":{"date-parts":[[2017,2,3]],"date-time":"2017-02-03T20:25:30Z","timestamp":1486153530000},"page":"45-49","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["La pr\u00e9valence des microd\u00e9l\u00e9tions et microduplications pathog\u00e8nes r\u00e9currentes en diagnostic pr\u00e9natal doit-elle amener \u00e0 revoir l\u2019\u00e9volution des techniques de d\u00e9pistage non invasif\u00a0? L\u2019exemple de la r\u00e9gion 22q11.2"],"prefix":"10.1016","volume":"45","author":[{"given":"F.","family":"Vialard","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Rouillac-Le Sciellour","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Besseau-Ayasse","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Oheix","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B.","family":"Herv\u00e9","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D.","family":"Molina-Gomes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"10","key":"10.1016\/j.gofs.2016.12.014_bib0005","doi-asserted-by":"crossref","first-page":"976","DOI":"10.1002\/pd.3945","article-title":"Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000\u00a0pregnancies","volume":"32","author":"Shaffer","year":"2012","journal-title":"Prenat Diagn"},{"issue":"23","key":"10.1016\/j.gofs.2016.12.014_bib0010","doi-asserted-by":"crossref","first-page":"2175","DOI":"10.1056\/NEJMoa1203382","article-title":"Chromosomal microarray versus karyotyping for prenatal diagnosis","volume":"367","author":"Wapner","year":"2013","journal-title":"N Engl J Med"},{"issue":"6","key":"10.1016\/j.gofs.2016.12.014_bib0015","doi-asserted-by":"crossref","first-page":"610","DOI":"10.1002\/uog.12464","article-title":"Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis","volume":"41","author":"Hillman","year":"2013","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"1","key":"10.1016\/j.gofs.2016.12.014_bib0020","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1002\/uog.14695","article-title":"Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis","volume":"45","author":"Jansen","year":"2015","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"6","key":"10.1016\/j.gofs.2016.12.014_bib0025","doi-asserted-by":"crossref","first-page":"650","DOI":"10.1002\/uog.14880","article-title":"Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis","volume":"46","author":"Grande","year":"2015","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"7","key":"10.1016\/j.gofs.2016.12.014_bib0030","doi-asserted-by":"crossref","first-page":"1148","DOI":"10.1373\/clinchem.2011.180794","article-title":"Detection of microdeletion 22q11.2\u00a0in a fetus by next-generation sequencing of maternal plasma","volume":"58","author":"Jensen","year":"2012","journal-title":"Clin Chem"},{"issue":"2","key":"10.1016\/j.gofs.2016.12.014_bib0035","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1016\/j.ajhg.2012.12.006","article-title":"Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma","volume":"92","author":"Srinivasan","year":"2013","journal-title":"Am J Hum Genet"},{"issue":"3","key":"10.1016\/j.gofs.2016.12.014_bib0040","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1002\/uog.12364","article-title":"Meta-analysis of second-trimester markers for trisomy 21","volume":"41","author":"Agathokleous","year":"2013","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"1","key":"10.1016\/j.gofs.2016.12.014_bib0045","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1002\/uog.14636","article-title":"Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis","volume":"45","author":"Akolekar","year":"2015","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"1\u00a0Suppl.","key":"10.1016\/j.gofs.2016.12.014_bib0050","doi-asserted-by":"crossref","first-page":"210","DOI":"10.1590\/S1415-47572014000200007","article-title":"New microdeletion and microduplication syndromes: a comprehensive review","volume":"37","author":"Nevado","year":"2014","journal-title":"Genet Mol Biol"},{"key":"10.1016\/j.gofs.2016.12.014_bib0055","series-title":"22q11.2\u00a0deletion syndrome. GeneReviews\u00ae","author":"McDonald-McGinn","year":"2013"},{"issue":"8","key":"10.1016\/j.gofs.2016.12.014_bib0060","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1002\/pd.4613","article-title":"Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500\u00a0pregnancies","volume":"35","author":"Grati","year":"2015","journal-title":"Prenat Diagn"},{"issue":"5","key":"10.1016\/j.gofs.2016.12.014_bib0065","doi-asserted-by":"crossref","first-page":"500","DOI":"10.1002\/pd.2727","article-title":"Prenatal BACs-on-Beads: a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis","volume":"31","author":"Vialard","year":"2011","journal-title":"Prenat Diagn"},{"issue":"9","key":"10.1016\/j.gofs.2016.12.014_bib0070","doi-asserted-by":"crossref","first-page":"838","DOI":"10.1038\/ng.909","article-title":"A copy number variation morbidity map of developmental delay","volume":"43","author":"Cooper","year":"2011","journal-title":"Nat Genet"},{"issue":"1","key":"10.1016\/j.gofs.2016.12.014_bib0075","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1002\/pd.4478","article-title":"Prenatal diagnosis of 24\u00a0cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations","volume":"35","author":"Dupont","year":"2014","journal-title":"Prenat Diagn"},{"issue":"6","key":"10.1016\/j.gofs.2016.12.014_bib0080","doi-asserted-by":"crossref","first-page":"844","DOI":"10.1038\/ejhg.2015.219","article-title":"A French multicenter study of over 700\u00a0patients with 22q11\u00a0deletions diagnosed using FISH or aCGH","volume":"24","author":"Poirsier","year":"2016","journal-title":"Eur J Hum Genet"},{"issue":"5","key":"10.1016\/j.gofs.2016.12.014_bib0085","doi-asserted-by":"crossref","first-page":"424","DOI":"10.1002\/pd.4321","article-title":"A French collaborative survey of 272\u00a0fetuses with 22q11.2\u00a0deletion: ultrasound findings, fetal autopsies and pregnancy outcomes","volume":"34","author":"Besseau-Ayasse","year":"2014","journal-title":"Prenat Diagn"},{"issue":"6","key":"10.1016\/j.gofs.2016.12.014_bib0090","doi-asserted-by":"crossref","first-page":"869","DOI":"10.1016\/j.ajhg.2015.10.013","article-title":"Histone modifier genes alter conotruncal heart phenotypes in 22q11.2\u00a0deletion syndrome","volume":"97","author":"Guo","year":"2015","journal-title":"Am J Hum Genet"},{"issue":"2","key":"10.1016\/j.gofs.2016.12.014_bib0095","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1002\/uog.15754","article-title":"Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2\u00a0deletion syndrome","volume":"47","author":"Gross","year":"2015","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"6","key":"10.1016\/j.gofs.2016.12.014_bib0100","doi-asserted-by":"crossref","first-page":"1330","DOI":"10.1097\/AOG.0000000000000874","article-title":"Cell-free DNA analysis in maternal plasma in cases of fetal abnormalities detected on ultrasound examination","volume":"125","author":"Benachi","year":"2015","journal-title":"Obstet Gynecol"}],"container-title":["Gyn\u00e9cologie Obst\u00e9trique Fertilit\u00e9 & S\u00e9nologie\u00a0"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2468718916300149?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2468718916300149?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2021,11,6]],"date-time":"2021-11-06T22:00:43Z","timestamp":1636236043000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2468718916300149"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,1]]},"references-count":20,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2017,1]]}},"alternative-id":["S2468718916300149"],"URL":"https:\/\/doi.org\/10.1016\/j.gofs.2016.12.014","relation":{},"ISSN":["2468-7189"],"issn-type":[{"value":"2468-7189","type":"print"}],"subject":[],"published":{"date-parts":[[2017,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"La pr\u00e9valence des microd\u00e9l\u00e9tions et microduplications pathog\u00e8nes r\u00e9currentes en diagnostic pr\u00e9natal doit-elle amener \u00e0 revoir l\u2019\u00e9volution des techniques de d\u00e9pistage non invasif\u00a0? L\u2019exemple de la r\u00e9gion 22q11.2","name":"articletitle","label":"Article Title"},{"value":"Gyn\u00e9cologie Obst\u00e9trique Fertilit\u00e9 & S\u00e9nologie\u00a0","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.gofs.2016.12.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"https:\/\/doi.org\/10.1016\/j.gofs.2016.12.013","name":"associatedlink","label":"CrossRef DOI link to the associated document"},{"value":"https:\/\/doi.org\/10.1016\/j.gofs.2016.12.012","name":"associatedlink","label":"CrossRef DOI link to the associated document"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}