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Article

The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human.

The Journal of clinical endocrinology and metabolism - 1 Dec 1996

Waldstreicher J, Seminara S B, Jameson J L, Geyer A, Nachtigall L B, Boepple P A, Holmes L B, Crowley W F

Abstract excerpt

Despite recent advances in the understanding of the pathophysiology of Kallmann's syndrome (KS), the patterns of inheritance in the majority of cases of GnRH deficiency in human subjects remain unclear. To define further the genetic and phenotypic variability of this syndrome, detailed family his...

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Source

Identifiers

PMID: 8954047
DOI: 10.1210/jcem.81.12.8954047

Genes

IHH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-8954047-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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