{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,4]],"date-time":"2025-10-04T06:12:07Z","timestamp":1759558327759,"version":"build-2065373602"},"reference-count":5,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,4,1]],"date-time":"2017-04-01T00:00:00Z","timestamp":1491004800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2017,4,1]],"date-time":"2017-04-01T00:00:00Z","timestamp":1491004800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","ejog.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["European Journal of Obstetrics &amp; Gynecology and Reproductive Biology"],"published-print":{"date-parts":[[2017,4]]},"DOI":"10.1016\/j.ejogrb.2017.02.025","type":"journal-article","created":{"date-parts":[[2017,2,24]],"date-time":"2017-02-24T22:19:26Z","timestamp":1487974766000},"page":"225-227","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"special_numbering":"C","title":["Whole-exome sequencing identifies compound heterozygous LHX4 mutations in a fetus with early-onset growth restriction"],"prefix":"10.1016","volume":"211","author":[{"given":"Yue-Cheng","family":"Lu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lv-Ying","family":"Huang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jin-Mei","family":"Yan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yi","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dong-Zhi","family":"Li","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ejogrb.2017.02.025_bib0005","doi-asserted-by":"crossref","first-page":"686","DOI":"10.1002\/pd.4844","article-title":"Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction","volume":"36","author":"Zhu","year":"2016","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.ejogrb.2017.02.025_bib0010","doi-asserted-by":"crossref","first-page":"144","DOI":"10.1006\/geno.1997.4852","article-title":"Lhx4, a LIM homeobox gene","volume":"44","author":"Yamashita","year":"1997","journal-title":"Genomics"},{"key":"10.1016\/j.ejogrb.2017.02.025_bib0015","first-page":"265","article-title":"Roles of the LHX3 and LHX 4 LIM-homeodomain factors in pituitary development","author":"Mullen","year":"2007","journal-title":"Mol Cell Endocrinol"},{"key":"10.1016\/j.ejogrb.2017.02.025_bib0020","first-page":"749","article-title":"LHX4 gene alterations: patient report and review of the literature","volume":"13","author":"Gucev","year":"2016","journal-title":"Pediatr Endocrinol Rev"},{"key":"10.1016\/j.ejogrb.2017.02.025_bib0025","doi-asserted-by":"crossref","first-page":"2158","DOI":"10.1210\/jc.2014-4484","article-title":"Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation","volume":"100","author":"Gregory","year":"2015","journal-title":"J Clin Endocrinol Metab"}],"container-title":["European Journal of Obstetrics &amp; Gynecology and Reproductive Biology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0301211517300969?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0301211517300969?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,4]],"date-time":"2025-10-04T05:40:30Z","timestamp":1759556430000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0301211517300969"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,4]]},"references-count":5,"alternative-id":["S0301211517300969"],"URL":"https:\/\/doi.org\/10.1016\/j.ejogrb.2017.02.025","relation":{},"ISSN":["0301-2115"],"issn-type":[{"type":"print","value":"0301-2115"}],"subject":[],"published":{"date-parts":[[2017,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Whole-exome sequencing identifies compound heterozygous LHX4 mutations in a fetus with early-onset growth restriction","name":"articletitle","label":"Article Title"},{"value":"European Journal of Obstetrics & Gynecology and Reproductive Biology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejogrb.2017.02.025","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}