Harvard Catalyst Profiles

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Mutations in Fibroblast Growth Factor-1 gene (FGFR1) occur in 8% of cases with normosmic idiopathic hypogonadotropic hypogonadism (nIHH)

Mutations in Fibroblast Growth Factor-1 gene (FGFR1) occur in 8% of cases with normosmic idiopathic hypogonadotropic hypogonadism (nIHH). Abstract OR52-4, p154, Program of the 88th Annual Meeting of the Endocrine Society, Boston. 2006.


Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.