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bn:02868430n
Noun Concept
PT
No term available
EN
46,XX/46,XY is a chimeric genetic condition characterized by the presence of some cells that express a 46,XX karyotype and some cells that express a 46,XY karyotype in a single human being. Wikipedia
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Sources
IS A
hermafroditismo
doença rara
EN
Sex chromosome anomalies
quimerismo

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