The molecular basis of inherited reproductive disorders

Study ID Alternative Stable ID Type
phs000475 Probands

Study Description

The purpose of this study is to discover genetic mutations in patients who have GnRH deficient states. This includes individuals with variant forms of hypogonadotropic hypogonadism, including individuals who have somatic anomalies involving mid-line facial defects, renal agenesis, synkinesia, and ataxia, amongst others.

Archive Link Archive Accession
dbGaP phs000475

Who archives the data?

There are no publications available