{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,28]],"date-time":"2025-10-28T18:19:34Z","timestamp":1761675574918,"version":"build-2065373602"},"reference-count":22,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2007,12,1]],"date-time":"2007-12-01T00:00:00Z","timestamp":1196467200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2007,12,1]],"date-time":"2007-12-01T00:00:00Z","timestamp":1196467200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.fr","em-consulte.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Transfusion Clinique et Biologique"],"published-print":{"date-parts":[[2007,12]]},"DOI":"10.1016\/j.tracli.2008.03.007","type":"journal-article","created":{"date-parts":[[2008,4,24]],"date-time":"2008-04-24T11:02:58Z","timestamp":1209034978000},"page":"568-571","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":10,"title":["Fetal RhD genotyping: A more efficient use of anti-D immunoglobulin"],"prefix":"10.1016","volume":"14","author":[{"given":"G.","family":"Daniels","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.","family":"Finning","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Martin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Summers","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"year":"2002","series-title":"Human Blood Groups","author":"Daniels","key":"10.1016\/j.tracli.2008.03.007_bib1"},{"key":"10.1016\/j.tracli.2008.03.007_bib2","doi-asserted-by":"crossref","first-page":"3662","DOI":"10.1182\/blood.V95.12.3662.012k12_3662_3668","article-title":"RHD gene deletion occurred in the Rhesus box","volume":"95","author":"Wagner","year":"2000","journal-title":"Blood"},{"key":"10.1016\/j.tracli.2008.03.007_bib3","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1182\/blood.V95.1.12","article-title":"The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in most Africans with the Rh D-negative blood group phenotype","volume":"95","author":"Singleton","year":"2000","journal-title":"Blood"},{"key":"10.1016\/j.tracli.2008.03.007_bib4","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1046\/j.1537-2995.1997.37197176949.x","article-title":"Molecular background of VS and weak C expression in blacks","volume":"37","author":"Faas","year":"1997","journal-title":"Transfusion"},{"key":"10.1016\/j.tracli.2008.03.007_bib5","doi-asserted-by":"crossref","first-page":"951","DOI":"10.1046\/j.1537-2995.1998.381098440860.x","article-title":"The Rh VS and V blood group polymorphisms in Africans: a serological and molecular analysis","volume":"38","author":"Daniels","year":"1998","journal-title":"Transfusion"},{"key":"10.1016\/j.tracli.2008.03.007_bib6","doi-asserted-by":"crossref","first-page":"385","DOI":"10.1182\/blood.V93.1.385","article-title":"Molecular basis of weak D phenotypes","volume":"93","author":"Wagner","year":"1999","journal-title":"Blood"},{"issue":"1S","key":"10.1016\/j.tracli.2008.03.007_bib7","first-page":"17S","article-title":"Rh complexities: serology and DNA genotyping","volume":"47","author":"Westhoff","year":"2007","journal-title":"Transfusion"},{"key":"10.1016\/j.tracli.2008.03.007_bib8","doi-asserted-by":"crossref","first-page":"1129","DOI":"10.1182\/blood.V83.4.1129.1129","article-title":"Rearrangements of the blood group RhD gene associated with the DVI category phenotype","volume":"83","author":"Mouro","year":"1994","journal-title":"Blood"},{"key":"10.1016\/j.tracli.2008.03.007_bib9","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1097\/00001703-200004000-00005","article-title":"Amniocentesis and chorionic villus sampling","volume":"12","author":"Wilson","year":"2000","journal-title":"Curr Opin Obstet Gynecol"},{"key":"10.1016\/j.tracli.2008.03.007_bib10","doi-asserted-by":"crossref","first-page":"528","DOI":"10.1111\/j.1471-0528.1987.tb03145.x","article-title":"Fetomaternal haemorrhage associated with genetic amniocentesis: results of a randomized trial","volume":"94","author":"Tabor","year":"1987","journal-title":"Br J Obstet Gynaecol"},{"key":"10.1016\/j.tracli.2008.03.007_bib11","doi-asserted-by":"crossref","first-page":"768","DOI":"10.1086\/301800","article-title":"Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis","volume":"62","author":"Lo","year":"1998","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tracli.2008.03.007_bib12","first-page":"32","article-title":"Prenatal typing of Rh and Kell blood group antigens: the edge of a watershed","volume":"17","author":"van der Schoot","year":"2003","journal-title":"Transfus Med Rev"},{"key":"10.1016\/j.tracli.2008.03.007_bib13","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1111\/j.1423-0410.2004.00569.x","article-title":"Fetal blood group genotyping from DNA from maternal plasma: an important advance in the management and prevention of haemolytic disease of the fetus and newborn","volume":"87","author":"Daniels","year":"2004","journal-title":"Vox Sang"},{"key":"10.1016\/j.tracli.2008.03.007_bib14","doi-asserted-by":"crossref","first-page":"1163","DOI":"10.1016\/j.ajog.2006.07.033","article-title":"Diagnostic accuracy of noninvasive fetal 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.tracli.2008.03.007_bib15","doi-asserted-by":"crossref","first-page":"1079","DOI":"10.1046\/j.1537-2995.2002.00165.x","article-title":"Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service","volume":"42","author":"Finning","year":"2002","journal-title":"Transfusion"},{"key":"10.1016\/j.tracli.2008.03.007_bib16","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1196\/annals.1368.011","article-title":"Fetal blood group genotyping. Present and future","volume":"1075","author":"Daniels","year":"2006","journal-title":"Ann N Y Acad Sci"},{"key":"10.1016\/j.tracli.2008.03.007_bib17","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1196\/annals.1368.016","article-title":"Use of bi-allelic insertion\/deletion polymorphisms as a positive control in maternal blood. First clinical experience","volume":"1075","author":"Page-Christiaens","year":"2006","journal-title":"Ann N Y Acad Sci"},{"key":"10.1016\/j.tracli.2008.03.007_bib18","doi-asserted-by":"crossref","first-page":"2211","DOI":"10.1373\/clinchem.2006.074997","article-title":"Hypermethylated RASSF1A in maternal plasma: a universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis","volume":"52","author":"Chan","year":"2006","journal-title":"Clin Chem"},{"key":"10.1016\/j.tracli.2008.03.007_bib19","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1111\/j.1423-0410.2005.00603.x","article-title":"Report of the first international workshop on molecular blood group genotyping","volume":"88","author":"Daniels","year":"2005","journal-title":"Vox Sang"},{"key":"10.1016\/j.tracli.2008.03.007_bib20","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1111\/j.1423-0410.2007.00926.x","article-title":"Report of the Second International Workshop on molecular blood group genotyping","volume":"93","author":"Daniels","year":"2007","journal-title":"Vox Sang"},{"key":"10.1016\/j.tracli.2008.03.007_bib21","doi-asserted-by":"crossref","unstructured":"Finning K, Martin P, Summers J, Massey E, Poole G, Daniels G. Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study. Brit Med J 2008; in press and http:\/\/www.bmj.com\/cgi\/content\/full\/bmj.39518.463206.25.","DOI":"10.1136\/bmj.39518.463206.25"},{"issue":"suppl 3","key":"10.1016\/j.tracli.2008.03.007_bib22","first-page":"9","article-title":"Screening for foetal RHD-genotype by plasma PCR in all D negative pregnant women is feasible","volume":"87","author":"van der Schoot","year":"2004","journal-title":"Vox Sang"}],"container-title":["Transfusion Clinique et Biologique"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1246782008000487?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1246782008000487?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T10:30:22Z","timestamp":1761129022000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1246782008000487"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,12]]},"references-count":22,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2007,12]]}},"alternative-id":["S1246782008000487"],"URL":"https:\/\/doi.org\/10.1016\/j.tracli.2008.03.007","relation":{},"ISSN":["1246-7820"],"issn-type":[{"type":"print","value":"1246-7820"}],"subject":[],"published":{"date-parts":[[2007,12]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Fetal RhD genotyping: A more efficient use of anti-D immunoglobulin","name":"articletitle","label":"Article Title"},{"value":"Transfusion Clinique et Biologique","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.tracli.2008.03.007","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2008 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}