{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T13:25:56Z","timestamp":1791206756339,"version":"4.1.0"},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1996,4,1]]},"DOI":"10.1093\/hmg\/5.4.509","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T22:20:49Z","timestamp":1027722049000},"page":"509-512","source":"Crossref","is-referenced-by-count":150,"title":["Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)"],"prefix":"10.1093","volume":"5","author":[{"given":"F","family":"Rousseau","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","container-title":["Human Molecular Genetics"],"original-title":[],"link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/5\/4\/509\/1613699\/5-4-509.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,23]],"date-time":"2017-08-23T05:09:28Z","timestamp":1503464968000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/5.4.509"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,4,1]]},"references-count":0,"journal-issue":{"issue":"4"},"URL":"https:\/\/doi.org\/10.1093\/hmg\/5.4.509","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[1996,4,1]]}}}