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Article

Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism.

Journal of endocrinological investigation - 1 Feb 2017

Bonomi M, Rochira V, Pasquali D, Balercia G, Jannini E A, Ferlin A

Abstract excerpt

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 be fully understood. By improving our knowledge on the role of some genetic aspects as well as on the KS, patients'...

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Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27644703
DOI: 10.1007/s40618-016-0541-6
PMCID: PMC5269463

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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