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We suggest that this condition be labelled OFD IV.<\/jats:p>","DOI":"10.1136\/jmg.21.3.189","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:09:16Z","timestamp":1226329756000},"page":"189-192","source":"Crossref","is-referenced-by-count":47,"title":["Orofaciodigital syndrome with mesomelic limb shortening."],"prefix":"10.1136","volume":"21","author":[{"given":"J","family":"Burn","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C","family":"Dezateux","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C M","family":"Hall","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M","family":"Baraitser","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1984,6,1]]},"reference":[{"key":"ref_1","article-title":"Recognizable patterns ofhuman malformation","author":"Smith, D.W.","year":"1982","unstructured":"Smith DW. 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J Pediatr 1967;71:94-102.","journal-title":"J Pediatr"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"377","DOI":"10.14219\/jada.archive.1974.0381","article-title":"Mohr syndrome or oral-facialdigital II: report of two cases","volume":"89","author":"Goldstein, E.; Medina, J.L.","year":"1974","unstructured":"Goldstein E, Medina JL. Mohr syndrome or oral-facialdigital II: report of two cases. JAm Dent Assoc 1974;89: 377-82.","journal-title":"JAm Dent Assoc"},{"key":"ref_5","article-title":"The genetics of hand malformations. Birth Defects 1978; XIV: No 3","author":"Temtamy, S.; McKusick, V.A.","unstructured":"Temtamy S, McKusick VA. The genetics of hand malformations. Birth Defects 1978;XIV: No 3."},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1136\/jmg.20.1.65","article-title":"A female infant wilh features of Mohr and Majewski syndromes: variable expression, a genetic compound, or a distinct entity?","volume":"20","author":"Baraitser, M.; Burn, J.; Fixsen, J.","year":"1983","unstructured":"Baraitser M, Burn J, Fixsen J. A female infant wilh features of Mohr and Majewski syndromes: variable expression, a genetic compound, or a distinct entity? J Med Genet 1983;20:65-7.","journal-title":"J Med Genet"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.21.3.189","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,17]],"date-time":"2025-10-17T20:16:05Z","timestamp":1760732165000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.21.3.189"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1984,6]]},"references-count":6,"journal-issue":{"issue":"3","published-online":{"date-parts":[[1984,6,1]]},"published-print":{"date-parts":[[1984,6]]}},"alternative-id":["10.1136\/jmg.21.3.189"],"URL":"https:\/\/doi.org\/10.1136\/jmg.21.3.189","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"value":"0022-2593","type":"print"},{"value":"1468-6244","type":"electronic"}],"subject":[],"published":{"date-parts":[[1984,6]]}}}