{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,5,9]],"date-time":"2024-05-09T05:05:41Z","timestamp":1715231141528},"reference-count":9,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":5542,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1990,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report on 3 brothers with hypertelorism, hypospadias, and tetralogy of Fallot. Parents are first cousins once removed; the father has apparent hypertelorism. An apparently normal paternal uncle who is married to a second cousin also has a daughter with hypertelorism and tetralogy of Fallot. All similarly affected relatives have mild or borderline mental retardation. The combination of anomalies may represent a previously undescribed autosomal recessive disorder.<\/jats:p>","DOI":"10.1002\/ajmg.1320350414","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T03:44:37Z","timestamp":1118547877000},"page":"516-518","source":"Crossref","is-referenced-by-count":9,"title":["Autosomal recessive inheritance of a syndrome of hypertelorism, hypospadias, and tetralogy of Fallot?"],"prefix":"10.1002","volume":"35","author":[{"given":"Talaat I.","family":"Farag","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ahmad S.","family":"Teebi","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":"10.1002\/ajmg.1320310319"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320280207"},{"key":"e_1_2_1_4_1","unstructured":"FriasJL RobertsSF McReynoldsJW CondronC(1983):Occurrence of the Opitz and the Opitz\u2010Frias syndromes in the same family. David Smith Morphogenesis Meeting (abstract)."},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320300323"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320280203"},{"key":"e_1_2_1_7_1","series-title":"BD:OAS","first-page":"86","volume-title":"The Clinical Delineation of Birth Defects Part II. Malformation syndromes","author":"Opitz JM","year":"1969"},{"key":"e_1_2_1_8_1","series-title":"BD:OAS","first-page":"95","volume-title":"The Clinical Delineation of Birth Defects. Part II. Malformation Syndromes","author":"Opitz JM","year":"1969"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.25.8.536"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.25.3.157"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320350414","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320350414","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,22]],"date-time":"2023-10-22T10:59:29Z","timestamp":1697972369000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320350414"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1990,4]]},"references-count":9,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1990,4]]}},"alternative-id":["10.1002\/ajmg.1320350414"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320350414","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1990,4]]}}}