{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T18:40:42Z","timestamp":1789756842221,"version":"4.0.1"},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2000,2,12]]},"DOI":"10.1093\/hmg\/9.3.367","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T18:22:25Z","timestamp":1027707745000},"page":"367-374","source":"Crossref","is-referenced-by-count":170,"title":["Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus"],"prefix":"10.1093","volume":"9","author":[{"given":"B. A.","family":"Bejjani","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\/9\/3\/367\/9815134\/090367.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,23]],"date-time":"2017-08-23T03:22:52Z","timestamp":1503458572000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/9.3.367"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,2,12]]},"references-count":0,"journal-issue":{"issue":"3"},"URL":"https:\/\/doi.org\/10.1093\/hmg\/9.3.367","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[2000,2,12]]}}}