{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T01:40:45Z","timestamp":1791855645356,"version":"4.3.4"},"reference-count":4,"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":5693,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1989,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Setleis syndrome, an autosomal recessive disorder characterized by \u201ccoarse\u201d face, temporal cutis aplasia, double upper eyelashes, absent lower eyelashes, chronic conjunctivitis, and prominent thick lips, was reported previously in 8 Puerto Rican children. We report on 3 unrelated children (one mentally retarded) with Setleis syndrome who are not of Puerto Rican descent. Two of our patients had imperforate anus, which has not previously been reported. The evolution of the phenotype over time is illustrated.<\/jats:p>","DOI":"10.1002\/ajmg.1320340311","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T03:32:04Z","timestamp":1118547124000},"page":"354-357","source":"Crossref","is-referenced-by-count":30,"title":["Expanded phenotype and ethnicity in Setleis syndrome"],"prefix":"10.1002","volume":"34","author":[{"given":"Robin Dawn","family":"Clark","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mahin","family":"Golabi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yves","family":"Lacassie","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bryan","family":"Hall","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Susan","family":"Seto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_1","first-page":"895","article-title":"Autosomal recessive inheritance in the Setleis bitemporal \u201cforceps marks\u201d syndrome","volume":"141","author":"Marion RW","year":"1987","journal-title":"Am J Dis Child"},{"key":"e_1_2_1_3_1","doi-asserted-by":"crossref","first-page":"615","DOI":"10.1001\/archderm.1974.01630100071018","article-title":"Bitemporal aplasia cutis congenita: Occurrence with other cutaneous abnormalities","volume":"110","author":"Rudolph RI","year":"1974","journal-title":"Arch Dermatol"},{"key":"e_1_2_1_4_1","doi-asserted-by":"crossref","first-page":"636","DOI":"10.1001\/archderm.1974.01630100084027","article-title":"Emendation to \u201cBitemporal aplasia cutis congenita.\u201d","volume":"110","author":"Rudolph RI","year":"1974","journal-title":"Arch Dermatol"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.32.4.540"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320340311","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320340311","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,22]],"date-time":"2023-10-22T18:19:25Z","timestamp":1697998765000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320340311"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,11]]},"references-count":4,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1989,11]]}},"alternative-id":["10.1002\/ajmg.1320340311"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320340311","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1989,11]]}}}