{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T09:47:33Z","timestamp":1762854453746,"version":"build-2065373602"},"reference-count":11,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2023,3,1]],"date-time":"2023-03-01T00:00:00Z","timestamp":1677628800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,3,1]],"date-time":"2023-03-01T00:00:00Z","timestamp":1677628800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,2,28]],"date-time":"2024-02-28T00:00:00Z","timestamp":1709078400000},"content-version":"am","delay-in-days":364,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,3,1]],"date-time":"2023-03-01T00:00:00Z","timestamp":1677628800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2023,3,1]],"date-time":"2023-03-01T00:00:00Z","timestamp":1677628800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2023,3,1]],"date-time":"2023-03-01T00:00:00Z","timestamp":1677628800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2023,3,1]],"date-time":"2023-03-01T00:00:00Z","timestamp":1677628800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2023,3,1]],"date-time":"2023-03-01T00:00:00Z","timestamp":1677628800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"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":[[2023,3]]},"DOI":"10.1016\/j.gofs.2022.11.147","type":"journal-article","created":{"date-parts":[[2022,11,30]],"date-time":"2022-11-30T11:38:23Z","timestamp":1669808303000},"page":"172-175","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"title":["Risque de trisomie 21\u00a0discordant en cas de marqueurs s\u00e9riques tr\u00e8s bas\u00a0: \u00e0 propos de cinq cas de triplo\u00efdie digynique"],"prefix":"10.1016","volume":"51","author":[{"given":"E.","family":"Roland","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Voirin-Mathieu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Verchain","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Odaert","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Dreux","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"Renom","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.gofs.2022.11.147_bib0060","unstructured":"Arr\u00eat\u00e9 du 14\u00a0d\u00e9cembre 2018\u00a0modifiant l\u2019arr\u00eat\u00e9 du 23\u00a0juin 2009\u00a0modifi\u00e9 fixant les r\u00e8gles de bonnes pratiques en mati\u00e8re de d\u00e9pistage et de diagnostic pr\u00e9natals avec utilisation des marqueurs s\u00e9riques maternels de trisomie21. Journal Officiel de la R\u00e9publique Fran\u00e7aise, 20\u00a0d\u00e9cembre 2018."},{"key":"10.1016\/j.gofs.2022.11.147_bib0065","unstructured":"Dupont JM, Gatinois V, Kleinfinger P, Renom G, Satre V, Tapia S, et al. Recommandations pour le d\u00e9pistage des anomalies chromosomiques f\u0153tales par l\u2019\u00e9tude de l\u2019ADN libre circulant (ADNlc) http:\/\/www.eaclf.org\/docs\/GBP_ADNlc-V4.pdf (accessed 02\u00a0ao\u00fbt 2022)."},{"key":"10.1016\/j.gofs.2022.11.147_bib0070","doi-asserted-by":"crossref","first-page":"1209","DOI":"10.1002\/pd.2149","article-title":"Screening for triploidy by the risk algorithms for trisomies 21, 18\u00a0and 13\u00a0at 11\u00a0weeks to 13\u00a0weeks and 6\u00a0days of gestation","volume":"28","author":"Kagan","year":"2008","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.gofs.2022.11.147_bib0075","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1111\/j.1469-1809.1982.tb00714.x","article-title":"Human triploidy: relationship between parental origin of the additional haploid complement and development of partial hydatidiform mole","volume":"46","author":"Jacobs","year":"1982","journal-title":"Ann Hum Genet"},{"key":"10.1016\/j.gofs.2022.11.147_bib0080","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1002\/pd.898","article-title":"First-trimester nuchal translucency and maternal serum free \u03b2-hCG\u03b2 and PAPP-A can detect triploidy and determine the parental origin","volume":"24","author":"Yaron","year":"2004","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.gofs.2022.11.147_bib0085","doi-asserted-by":"crossref","first-page":"479","DOI":"10.1002\/pd.1170","article-title":"First-trimester screening for fetal triploidy at 11\u00a0to 14\u00a0weeks: a role for fetal biometry","volume":"25","author":"Salomon","year":"2005","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.gofs.2022.11.147_bib0090","doi-asserted-by":"crossref","first-page":"530","DOI":"10.1002\/uog.12460","article-title":"Detection of triploidy at 11-14weeks gestation: a cohort study of 198 000\u00a0pregnant women","volume":"42","author":"Engelbrechtsen","year":"2013","journal-title":"Ultrasound Obstet Gynecol"},{"key":"10.1016\/j.gofs.2022.11.147_bib0095","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1002\/pd.1115","article-title":"Triploidy identified through second-trimester serum screening","volume":"25","author":"Huang","year":"2005","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.gofs.2022.11.147_bib0100","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1111\/cge.14003","article-title":"Triploid pregnancy-Clinical implications","volume":"100","author":"Massalska","year":"2021","journal-title":"Clin Genet"},{"key":"10.1016\/j.gofs.2022.11.147_bib0105","doi-asserted-by":"crossref","first-page":"671","DOI":"10.1016\/j.jgyn.2014.05.012","article-title":"ABA. D\u00e9pistage de la trisomie 21\u00a0par les marqueurs s\u00e9riques maternels: justification des commentaires appliqu\u00e9s par les biologistes","volume":"9","author":"Muller","year":"2014","journal-title":"J Gynecol Obstet Biol Reprod"},{"key":"10.1016\/j.gofs.2022.11.147_bib0055","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":"2012","journal-title":"NEJM"}],"container-title":["Gyn\u00e9cologie Obst\u00e9trique Fertilit\u00e9 & S\u00e9nologie\u00a0"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2468718922004834?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2468718922004834?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T09:42:56Z","timestamp":1762854176000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2468718922004834"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,3]]},"references-count":11,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2023,3]]}},"alternative-id":["S2468718922004834"],"URL":"https:\/\/doi.org\/10.1016\/j.gofs.2022.11.147","relation":{},"ISSN":["2468-7189"],"issn-type":[{"type":"print","value":"2468-7189"}],"subject":[],"published":{"date-parts":[[2023,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Risque de trisomie 21\u00a0discordant en cas de marqueurs s\u00e9riques tr\u00e8s bas\u00a0: \u00e0 propos de cinq cas de triplo\u00efdie digynique","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.2022.11.147","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2022 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}