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Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism
Klinefelter Syndrome (KS) is characterized by an extreme heterogeneity in its clinical and genetic presentation. The relationship between clinical phenotype and genetic background has been partially disclosed; nevertheless, physicians are aware that several aspects concerning this issue are far to b...
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| Publicado no: | J Endocrinol Invest |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5269463/ https://ncbi.nlm.nih.gov/pubmed/27644703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40618-016-0541-6 |
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