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Brain Magnetic Resonance Imaging Findings in 49,XXXXY Syndrome
Klinefelter syndrome is a chromosomal disorder characterized by one or more supernumerary X chromosomes, in addition to the normal 46,XY male karyotype. Whereas classic Klinefelter syndrome (47,XXY) occurs in 1:400 births, the most severe Klinefelter variant (49,XXXXY) occurs in only 1:85,000 births...
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| I publikationen: | Pediatr Neurol |
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| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2008
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4369151/ https://ncbi.nlm.nih.gov/pubmed/18486832 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pediatrneurol.2008.03.004 |
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