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

Abstract

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 histories were reviewed in 106 cases of GnRH deficiency with or… (More)

Topics

Figures and Tables

Sorry, we couldn't extract any figures or tables for this paper.