<p>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. </p>

The Molecular Basis of Inherited Reproductive Disorders

Hypogonadism study with SNP Genotypes (NGS), WXS data on dbGaP (1 participants)

The Molecular Basis of Inherited Reproductive Disorders

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