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On the basis of this experience we examine the diagnostic criteria for the presumed autosomal recessive trigonocephaly C syndrome.<\/jats:p>","DOI":"10.1136\/jmg.22.1.39","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:09:16Z","timestamp":1226329756000},"page":"39-45","source":"Crossref","is-referenced-by-count":60,"title":["Trigonocephaly and the Opitz C syndrome."],"prefix":"10.1136","volume":"22","author":[{"given":"C","family":"Sargent","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Burn","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Baraitser","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M E","family":"Pembrey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1985,2,1]]},"reference":[{"key":"ref_1","first-page":"1862","article-title":"Untersuchungen uber wachstum und bau des menschlichen schadels","author":"Welcker, H.","unstructured":"Welcker H. 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Atlas des maladies chromosomiques. 2nd ed. Paris: Expansion Scientifique Frangaise, 1982.","edition":"2nd ed"},{"key":"ref_5","article-title":"Chromosomal variation in man. A catalog of chromosomal variants and anomalies","author":"Borgaonkar, D.S.","year":"1980","unstructured":"Borgaonkar DS. Chromosomal variation in man. A catalog of chromosomal variants and anomalies. 3rd ed. New York: Liss, 1980.","edition":"3rd ed"},{"key":"ref_6","first-page":"161","article-title":"The C syndrome of multiple congenital anomalies","volume":"2","author":"Opitz, J.M.; Johnson, R.C.; McCreadie, SR, Smith; D.W.","year":"1969","unstructured":"Opitz JM, Johnson RC, McCreadie SR, Smith DW. The C syndrome of multiple congenital anomalies. Birth Defects 1969;V(2):161-6.","journal-title":"Birth Defects"},{"key":"ref_7","first-page":"58","article-title":"The 'C' syndrome","volume":"2","author":"Preus, M.; Alexander, W.J.; Fraser, F.C.","year":"1975","unstructured":"Preus M, Alexander WJ, Fraser FC. 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Philadelphia: Saunders, 1981."}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.22.1.39","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,5]],"date-time":"2025-10-05T18:54:36Z","timestamp":1759690476000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.22.1.39"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1985,2]]},"references-count":10,"journal-issue":{"issue":"1","published-online":{"date-parts":[[1985,2,1]]},"published-print":{"date-parts":[[1985,2]]}},"alternative-id":["10.1136\/jmg.22.1.39"],"URL":"https:\/\/doi.org\/10.1136\/jmg.22.1.39","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"type":"print","value":"0022-2593"},{"type":"electronic","value":"1468-6244"}],"subject":[],"published":{"date-parts":[[1985,2]]}}}