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Severe myelinopathy in 49,XXXXY syndrome
49,XXXXY is a rare aneuploidy with neuroanatomic findings scarcely reported in the literature. Given the fact that many of its phenotypic characteristics are similar to Klinefelter patients, 49,XXXXY has been treated as a variant of Klinefelter syndrome in the past. Newer studies have shown that int...
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| Pubblicato in: | Neuroradiol J |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
SAGE Publications
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6136133/ https://ncbi.nlm.nih.gov/pubmed/28627968 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1971400917703989 |
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