{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,29]],"date-time":"2025-09-29T15:37:31Z","timestamp":1759160251282},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1998,4,1]]},"DOI":"10.1093\/hmg\/7.4.629","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T22:35:07Z","timestamp":1027722907000},"page":"629-635","source":"Crossref","is-referenced-by-count":25,"title":["ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene"],"prefix":"10.1093","volume":"7","author":[{"given":"E.","family":"Lindsay","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","container-title":["Human Molecular Genetics"],"original-title":[],"link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/7\/4\/629\/2672235\/7-4-629.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,23]],"date-time":"2017-08-23T16:56:29Z","timestamp":1503507389000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/7.4.629"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1998,4,1]]},"references-count":0,"journal-issue":{"issue":"4"},"URL":"https:\/\/doi.org\/10.1093\/hmg\/7.4.629","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[1998,4,1]]}}}