Associated Papers
Identification of a Novel Nonsense Mutation in the IGSF1 Gene Reveals Sex-Specific Phenotypic Variability Within a Single Family.
Ruta R et al.
Children (basel, Switzerland), 2025
Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.
Malcher A et al.
Andrology, 2022
Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.
Tenenbaum-Rakover Y et al.
Thyroid : Official Journal of the American Thyroid Association, 2016
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