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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Detalles Bibliográficos
Autores principales: Bonomi, M., Rochira, V., Pasquali, D., Balercia, G., Jannini, E. A., Ferlin, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Short Review
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

Internet

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

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