{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,3]],"date-time":"2023-10-03T16:11:30Z","timestamp":1696349490557},"reference-count":12,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2015,5,5]],"date-time":"2015-05-05T00:00:00Z","timestamp":1430784000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European J of Haematology"],"published-print":{"date-parts":[[2015,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A 62\u2010yr\u2010old man with two healthy daughters was diagnosed with osteomyelofibrosis. To our surprise, a female <jats:styled-content style=\"fixed-case\">XX<\/jats:styled-content>\u2010karyotype was observed in bone marrow and confirmed in <jats:styled-content style=\"fixed-case\">PHA<\/jats:styled-content>\u2010stimulated T\u2010lymphocytes from peripheral blood. Further molecular genetic investigation revealed a submicroscopic translocation between the short arm of X and Y, which leads to an <jats:styled-content style=\"fixed-case\">XX<\/jats:styled-content>\u2010male genotype based on an unbalanced translocation X;Y. This rare coincidence was further accentuated as the <jats:styled-content style=\"fixed-case\">USP<\/jats:styled-content>9Y gene, suspected to be to be involved in sperm cell production, was absent, but no azoospermia was present. In general, routine cytogenetics may result in findings that need to be further delineated and, as here, lead to a rare observation.<\/jats:p>","DOI":"10.1111\/ejh.12555","type":"journal-article","created":{"date-parts":[[2015,3,25]],"date-time":"2015-03-25T15:19:41Z","timestamp":1427296781000},"page":"254-256","source":"Crossref","is-referenced-by-count":1,"title":["Primary osteomyelofibrosis and an <scp>XX<\/scp>\u2010male genotype"],"prefix":"10.1111","volume":"95","author":[{"given":"Julie","family":"Schanz","sequence":"first","affiliation":[{"name":"Department of Hematology and Medical Oncology University Medicine of G\u00f6ttingen G\u00f6ttingen Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Detlef","family":"Haase","sequence":"additional","affiliation":[{"name":"Department of Hematology and Medical Oncology University Medicine of G\u00f6ttingen G\u00f6ttingen Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Peter","family":"Steuernagel","sequence":"additional","affiliation":[{"name":"Institute of Clinical Genetics Klinikum Oldenburg Oldenburg Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katayoo","family":"Shirneshan","sequence":"additional","affiliation":[{"name":"Department of Hematology and Medical Oncology University Medicine of G\u00f6ttingen G\u00f6ttingen Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J\u00f6rg","family":"B\u00e4secke","sequence":"additional","affiliation":[{"name":"Department of Hematology and Oncology St. Josefs\u2010Hospital Cloppenburg Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2015,5,5]]},"reference":[{"key":"e_1_2_2_2_1","first-page":"375","article-title":"Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal\u2010derived SRY\u2010bearing X chromosome","volume":"316","author":"Abbas N","year":"1993","journal-title":"C R Acad Sci III"},{"key":"e_1_2_2_3_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-2001-15393"},{"key":"e_1_2_2_4_1","doi-asserted-by":"publisher","DOI":"10.1146\/annurev.ge.27.120193.000443"},{"key":"e_1_2_2_5_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00335-002-3068-4"},{"key":"e_1_2_2_6_1","doi-asserted-by":"publisher","DOI":"10.1071\/RD03002"},{"key":"e_1_2_2_7_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa0806218"},{"key":"e_1_2_2_8_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-0032-1329199"},{"key":"e_1_2_2_9_1","doi-asserted-by":"publisher","DOI":"10.1038\/nrneph.2012.259"},{"key":"e_1_2_2_10_1","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.e2707"},{"key":"e_1_2_2_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(05)71142-9"},{"key":"e_1_2_2_12_1","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2012-05-429696"},{"key":"e_1_2_2_13_1","doi-asserted-by":"publisher","DOI":"10.1038\/leu.2011.320"}],"container-title":["European Journal of Haematology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fejh.12555","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/ejh.12555","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,2]],"date-time":"2023-10-02T09:35:26Z","timestamp":1696239326000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/ejh.12555"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,5,5]]},"references-count":12,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2015,9]]}},"alternative-id":["10.1111\/ejh.12555"],"URL":"https:\/\/doi.org\/10.1111\/ejh.12555","archive":["Portico"],"relation":{},"ISSN":["0902-4441","1600-0609"],"issn-type":[{"value":"0902-4441","type":"print"},{"value":"1600-0609","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015,5,5]]}}}