{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T10:43:11Z","timestamp":1790073791944,"version":"4.0.1"},"reference-count":8,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,10,1]],"date-time":"2017-10-01T00:00:00Z","timestamp":1506816000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2017,10,1]],"date-time":"2017-10-01T00:00:00Z","timestamp":1506816000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2017,7,29]],"date-time":"2017-07-29T00:00:00Z","timestamp":1501286400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Case Reports in Women's Health"],"published-print":{"date-parts":[[2017,10]]},"DOI":"10.1016\/j.crwh.2017.09.003","type":"journal-article","created":{"date-parts":[[2017,10,2]],"date-time":"2017-10-02T12:16:30Z","timestamp":1506946590000},"page":"4-7","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":15,"special_numbering":"C","title":["Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis"],"prefix":"10.1016","volume":"16","author":[{"given":"Dawn M.","family":"Hannah","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Terry B.","family":"Tressler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claudia D.","family":"Taboada","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.crwh.2017.09.003_bb0005","first-page":"918","article-title":"Anemia and Pregnancy","author":"Kilpatrick","year":"2014"},{"key":"10.1016\/j.crwh.2017.09.003_bb0010","author":"Segel","year":"2016"},{"key":"10.1016\/j.crwh.2017.09.003_bb0015","doi-asserted-by":"crossref","first-page":"252","DOI":"10.1038\/sj.jp.7211657","article-title":"Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis","volume":"27","author":"Yetgin","year":"2007","journal-title":"J. Perinatol."},{"key":"10.1016\/j.crwh.2017.09.003_bb0020","doi-asserted-by":"crossref","first-page":"3043","DOI":"10.1182\/blood.V78.11.3043.3043","article-title":"Deficiency of \u03b1-spectrin synthesis in burst forming units-erythroid in lethal hereditary spherocytosis","volume":"78","author":"Whitfield","year":"1991","journal-title":"Blood"},{"key":"10.1016\/j.crwh.2017.09.003_bb0025","doi-asserted-by":"crossref","first-page":"1174","DOI":"10.1172\/JCI117766","article-title":"Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene","volume":"95","author":"Gallagher","year":"1995","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.crwh.2017.09.003_bb0030","first-page":"569","article-title":"Nonimmune hydrops","author":"Wilkins","year":"2014"},{"key":"10.1016\/j.crwh.2017.09.003_bb0035","doi-asserted-by":"crossref","first-page":"404","DOI":"10.1038\/jp.2012.67","article-title":"A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency","volume":"33","author":"Yaish","year":"2013","journal-title":"J. Perinatol."},{"key":"10.1016\/j.crwh.2017.09.003_bb0040","first-page":"913","article-title":"Hereditary spherocytosis, hereditary elliptocytosis, and other disorders associated with abnormalities of the erythrocyte membrane","author":"Gallagher","year":"2009"}],"container-title":["Case Reports in Women's Health"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2214911217300577?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2214911217300577?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T05:25:38Z","timestamp":1762406738000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2214911217300577"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,10]]},"references-count":8,"alternative-id":["S2214911217300577"],"URL":"https:\/\/doi.org\/10.1016\/j.crwh.2017.09.003","relation":{},"ISSN":["2214-9112"],"issn-type":[{"value":"2214-9112","type":"print"}],"subject":[],"published":{"date-parts":[[2017,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis","name":"articletitle","label":"Article Title"},{"value":"Case Reports in Women's Health","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.crwh.2017.09.003","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 The Authors. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}