{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,28]],"date-time":"2025-10-28T18:13:38Z","timestamp":1761675218632},"reference-count":13,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":7764,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1984,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We describe two unrelated patients with a severe form of acrofacial dysostosis. Facial defects in both include coloboma of the lids, micrognathia, lateral oral clefting, palatal clefting, and severe auricular anomalies, with one showing bilateral cleft lip and right oblique facial clefting as well. Both have absent forearms and thumbs. Lower limbs were severely reduced in both infants with the feet attached either to the femur or directly to the trunk. Parental consanguinity was present in one case. The condition in these two infants appears to represent either a severe form of Nager acrofacial dysostosis or a new type of acrofacial dysostosis.<\/jats:p>","DOI":"10.1002\/ajmg.1320170314","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T19:38:39Z","timestamp":1118518719000},"page":"641-647","source":"Crossref","is-referenced-by-count":35,"title":["Acrofacial dysostosis with severe facial clefting and limb reduction"],"prefix":"10.1002","volume":"17","author":[{"given":"E. L.","family":"Kawira","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D. D.","family":"Weaver","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H. A.","family":"Bender","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John M.","family":"Opitz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(77)80453-8"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(81)80546-X"},{"key":"e_1_2_1_4_1","first-page":"289","article-title":"Une observation familiale du syndrome ectrodactylie et sysostose mandibulo\u2010faciale","volume":"22","author":"Fontaine G","year":"1974","journal-title":"J G\u00e9n\u00e9t Hum"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(63)80233-4"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320140203"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9394(71)90862-2"},{"key":"e_1_2_1_8_1","first-page":"35","article-title":"Nager acrofacial dysostosis: Early intervention and long\u2010term planning","volume":"14","author":"Meyerson MD","year":"1977","journal-title":"Cleft Palate J"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(79)80285-1"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320120403"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320140204"},{"key":"e_1_2_1_12_1","first-page":"455","article-title":"Die Differentialdiagnose der radialen Defektbildungen","volume":"7","author":"Sch\u00f6nenberg H","year":"1968","journal-title":"Paediat Prax"},{"issue":"7","key":"e_1_2_1_13_1","first-page":"109","article-title":"Congenital absence of the radius with hemifacial microsomia, ventricular septal defect and crossed renal ectopia","author":"Sugiura Y","year":"1971","journal-title":"BD:OAS"},{"issue":"6","key":"e_1_2_1_14_1","first-page":"116A","article-title":"Nager syndrome with partial duplication of the long arm of chromosome 2","volume":"31","author":"Wagner SF","year":"1979","journal-title":"Am J Hum Genet"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320170314","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320170314","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,19]],"date-time":"2023-10-19T20:33:37Z","timestamp":1697747617000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320170314"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1984,3]]},"references-count":13,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1984,3]]}},"alternative-id":["10.1002\/ajmg.1320170314"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320170314","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1984,3]]}}}