{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T15:50:04Z","timestamp":1786636204030,"version":"build-2736575974"},"reference-count":10,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Lung India"],"published-print":{"date-parts":[[2010]]},"DOI":"10.4103\/0970-2113.68322","type":"journal-article","created":{"date-parts":[[2010,8,10]],"date-time":"2010-08-10T04:22:53Z","timestamp":1281414173000},"page":"176","source":"Crossref","is-referenced-by-count":7,"title":["Cleidocranial dysplasia"],"prefix":"10.4103","volume":"27","author":[{"given":"Ramakant","family":"Dixit","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kalpana","family":"Dixit","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"AR","family":"Paramez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"key-10.4103\/0970-2113.68322-1","unstructured":"Mendoza-Londono R, Lee B. Cleidocranial dysplasia. Gene reviews. p. 1-18. Available from: http:\/\/www.ncbi.nlm.gov\/bookshelf\/ br.fcgi?book=gene&part=ccd. [last update on 2009 June 25]."},{"key":"key-10.4103\/0970-2113.68322-2","first-page":"2311","volume-title":"CBFA1 mutation analysis and functional correlation with phenotypic variability in Cleidocranial dysplasia","author":"Zhou","year":"1999","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0970-2113.68322-3","first-page":"177","volume-title":"Cleidocranial dysplasia: Clinical and molecular genetics","author":"Mundlos","year":"1999","journal-title":"J Med Genet"},{"key":"key-10.4103\/0970-2113.68322-4","unstructured":"Yochum TR, Rowe LJ. Essentials of skeletal radiology, 2 nd ed. Baltimore: Williams and Wilkins; 1996. p. 589-92."},{"key":"key-10.4103\/0970-2113.68322-5","first-page":"1","volume-title":"A natural history of Cleidocranial dysplasia","author":"Coopper","year":"2001","journal-title":"Am J Med Genet"},{"key":"key-10.4103\/0970-2113.68322-6","first-page":"292","volume-title":"Intrafamilial variability in Cleidocranial dysplasia: A three generation family","author":"Chitayat","year":"1992","journal-title":"Am J Med Genet"},{"key":"key-10.4103\/0970-2113.68322-7","first-page":"5","volume-title":"Cleidocranial dysostosis: A review of 40 new cases","author":"Jarvis","year":"1974","journal-title":"Am J Roentgenol Radium Ther Nucl Med"},{"key":"key-10.4103\/0970-2113.68322-8","unstructured":"Taveras JM, Ferrucci JT. Radiology diagnosis: Imaging-intervention. Philadelphia: Lippincott-Raven; 1996. p. 565-68."},{"key":"key-10.4103\/0970-2113.68322-9","first-page":"185","volume-title":"Cleidocranial dysplasia: A case report","author":"Feldman","year":"2002","journal-title":"J Can Chiropr Assoc"},{"key":"key-10.4103\/0970-2113.68322-10","first-page":"225","volume-title":"Large fontanels are a shared features of haploinsufficiency of RUNX2 and its coactivator CBFB","author":"Goto","year":"2004","journal-title":"Congenit Anom"}],"container-title":["Lung India"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T14:54:51Z","timestamp":1786632891000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/0970-2113.68322"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010]]},"references-count":10,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2010]]}},"alternative-id":["68322"],"URL":"https:\/\/doi.org\/10.4103\/0970-2113.68322","relation":{},"ISSN":["0970-2113"],"issn-type":[{"value":"0970-2113","type":"print"}],"subject":[],"published":{"date-parts":[[2010]]}}}