{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,4]],"date-time":"2025-09-04T14:00:03Z","timestamp":1756994403948,"version":"3.40.4"},"reference-count":0,"publisher":"S. Karger AG","issue":"6","license":[{"start":{"date-parts":[[1964,1,1]],"date-time":"1964-01-01T00:00:00Z","timestamp":-189388800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"},{"start":{"date-parts":[[1964,1,1]],"date-time":"1964-01-01T00:00:00Z","timestamp":-189388800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cytogenet Genome Res"],"published-print":{"date-parts":[[1964]]},"abstract":"<jats:p>A sex chromatin positive woman has stunted growth, primary amenor-rhoea, cubitus valgus, Madelung\u2019s deformity and mental deficiency. A modal chromosome number of 46 was found in cultures from peripheral blood, skin and &lt;i&gt;Fascia lata, &lt;\/i&gt;but an abnormal very large metacentric chromosome and only 15 chromosomes in the X-6\u201312 group were observed in karyotypes from cells of all cultures. Large and characteristic bipartite bodies were often present in buccal and vaginal smears, and the size of the polymorphonuclear drumsticks was increased. Autoradiographically the abnormal chromosome was the only \u201chot\u201d chromosome. The patient was Xg&lt;sup&gt;a&lt;\/sup&gt; negative although her father was Xg&lt;sup&gt;a&lt;\/sup&gt; positive. We conclude that the unpaired large chromosome in our patient is an abnormal X chromosome with a partial deletion and a translocation of a piece of an autosome or sex chromosome onto its short arm.<\/jats:p>","DOI":"10.1159\/000129831","type":"journal-article","created":{"date-parts":[[2008,4,30]],"date-time":"2008-04-30T09:35:09Z","timestamp":1209548109000},"page":"427-440","source":"Crossref","is-referenced-by-count":20,"title":["A Very Large Metacentric Chromosome in a Woman with Symptoms of Turner\u2019s Syndrome"],"prefix":"10.1159","volume":"3","author":[{"given":"Gouw","family":"Wie Lie","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.M.","family":"Coenegracht","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"Stalder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"127","published-online":{"date-parts":[[2008,4,29]]},"container-title":["Cytogenetic and Genome Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.karger.com\/Article\/Pdf\/129831","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.karger.com\/Article\/Pdf\/129831","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,4,24]],"date-time":"2025-04-24T01:33:10Z","timestamp":1745458390000},"score":1,"resource":{"primary":{"URL":"https:\/\/karger.com\/article\/doi\/10.1159\/000129831"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1964]]},"references-count":0,"journal-issue":{"issue":"6","published-online":{"date-parts":[[2004,7,1]]}},"URL":"https:\/\/doi.org\/10.1159\/000129831","archive":["Portico"],"relation":{},"ISSN":["1424-8581","1424-859X"],"issn-type":[{"type":"print","value":"1424-8581"},{"type":"electronic","value":"1424-859X"}],"subject":[],"published":{"date-parts":[[1964]]}}}