Associated Papers
Shared genetics between nonobstructive azoospermia and primary ovarian insufficiency.
Verrilli L et al.
F&s Reviews, 2021
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.
Jolly A et al.
The Journal of Clinical Endocrinology and Metabolism, 2019
Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism.
Bayram Y et al.
The Journal of Clinical Endocrinology and Metabolism, 2015
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