{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T06:06:10Z","timestamp":1761717970845},"reference-count":20,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":7703,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1984,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>An unusual supernumerary chromosome with a single satellite on the long arm was found in a child with manifestations of the cat\u2010eye syndrome including apparently low\u2010set and malformed ears, preauricular tags, micrognathia, and imperforate anus. Although G\u2010banding suggested that this extra material was chromosome 22, this was not confirmed by several other banding techniques. After examination of the parents' chromosomes, the nature and origin of this extra chromosome remains obscure. We conclude that patients previously diagnosed as having \u201cpartial trisomy 22\u201d with incomplete cat\u2010eye syndrome may have a different chromosome constitution when studied by various banding techniques.<\/jats:p>","DOI":"10.1002\/ajmg.1320180105","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T19:41:50Z","timestamp":1118518910000},"page":"19-24","source":"Crossref","is-referenced-by-count":9,"title":["Cat\u2010eye syndrome with unusual marker chromosome probably not chromosome 22"],"prefix":"10.1002","volume":"18","author":[{"given":"Warren","family":"Rosenfeld","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ram S.","family":"Verma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ramesh C.","family":"Jhaveri","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":"10.1001\/archpedi.1977.02120210071015"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00295742"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.14.4.288"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00277580"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00281567"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1977.tb00895.x"},{"key":"e_1_2_1_8_1","first-page":"349","volume-title":"New Chromosomal Syndromes","author":"Hsu LY","year":"1977"},{"key":"e_1_2_1_9_1","series-title":"Birth Defects: Original Article Series","volume-title":"A Internation System for Human Cytogenetic Nomenclature","author":"ISCN","year":"1978"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00272188"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(65)92415-3"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00274675"},{"key":"e_1_2_1_13_1","first-page":"148","article-title":"The \u201ccat eye\u201d syndrome: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter \u2192 q11) associated with characteristic phenotype","volume":"57","author":"Schnizel A","year":"1981","journal-title":"Hum Genet"},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(71)90287-X"},{"key":"e_1_2_1_15_1","first-page":"60","volume-title":"Recognizable Patterns of Human Malformation","author":"Smith D","year":"1982"},{"key":"e_1_2_1_16_1","first-page":"77","article-title":"NSG banding of sequentially QFQ and RFA banded human chromosomes","volume":"55","author":"Ved\u2010Brat S","year":"1980","journal-title":"Stain Technol"},{"key":"e_1_2_1_17_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2818.1976.tb01107.x"},{"key":"e_1_2_1_18_1","first-page":"110","article-title":"A simple R\u2010banding technic","volume":"27","author":"Verma RS","year":"1975","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_19_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00330664"},{"key":"e_1_2_1_20_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320070412"},{"key":"e_1_2_1_21_1","doi-asserted-by":"publisher","DOI":"10.1177\/000992287601500706"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320180105","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320180105","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,19]],"date-time":"2023-10-19T22:35:01Z","timestamp":1697754901000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320180105"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1984,5]]},"references-count":20,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1984,5]]}},"alternative-id":["10.1002\/ajmg.1320180105"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320180105","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1984,5]]}}}