{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,2]],"date-time":"2026-05-02T23:06:25Z","timestamp":1777763185663,"version":"3.51.4"},"reference-count":0,"publisher":"S. Karger AG","license":[{"start":{"date-parts":[[2008,5,7]],"date-time":"2008-05-07T00:00:00Z","timestamp":1210118400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"},{"start":{"date-parts":[[2008,5,7]],"date-time":"2008-05-07T00:00:00Z","timestamp":1210118400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cytogenet Cell Genet"],"abstract":"<jats:p>The gene for red blood cell (RBC) catalase has recently been mapped to 11p13, and a gene dosage effect has been demonstrated for individuals with triplication or deletion of that region. Deletion of the 11pl3 band has also been associated with aniridia, with and without Wilms\u2019 tumor. We studied the RBC catalase levels in individuals without detectable chromosomal abnormalities but with aniridia, Wilms\u2019 tumor, and the combination of aniridia and Wilms\u2019 tumor, to determine whether catalase levels might provide evidence for a sub-microscopic chromosomal deletion in the 11p13 region. All karyotypically normal patients were found to have normal catalase levels.<\/jats:p>","DOI":"10.1159\/000131636","type":"journal-article","created":{"date-parts":[[2008,5,7]],"date-time":"2008-05-07T10:33:47Z","timestamp":1210156427000},"page":"120-123","source":"Crossref","is-referenced-by-count":21,"title":["Catalase levels in patients with aniridia and\/or Wilms\u2019 tumor: utility and limitations"],"prefix":"10.1159","author":[{"given":"R.E.","family":"Ferrell","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"V.M.","family":"Riccardi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"127","published-online":{"date-parts":[[2008,5,7]]},"container-title":["Cytogenetics and Cell Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.karger.com\/Article\/Pdf\/131636","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/karger.com\/article-pdf\/doi\/10.1159\/000131636","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T14:43:32Z","timestamp":1777473812000},"score":1,"resource":{"primary":{"URL":"https:\/\/karger.com\/article\/doi\/10.1159\/000131636"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,5,7]]},"references-count":0,"URL":"https:\/\/doi.org\/10.1159\/000131636","archive":["Portico"],"relation":{},"ISSN":["0301-0171","1421-9816"],"issn-type":[{"value":"0301-0171","type":"print"},{"value":"1421-9816","type":"electronic"}],"subject":[],"published":{"date-parts":[[2008,5,7]]}}}