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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer International Publishing
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269463/ https://www.ncbi.nlm.nih.gov/pubmed/27644703 http://dx.doi.org/10.1007/s40618-016-0541-6 |