Associated Papers
Whole Exome Sequencing Points towards a Multi-Gene Synergistic Action in the Pathogenesis of Congenital Combined Pituitary Hormone Deficiency.
Sertedaki A et al.
Cells, 2022
GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review.
Patil VA et al.
Neuroendocrinology, 2022
Central hypogonadotropic hypogonadism: genetic complexity of a complex disease.
Marino M et al.
International Journal of Endocrinology, 2014
A needle in a haystack: mutations in GNRH1 as a rare cause of isolated GnRH deficiency.
Chan YM
Molecular and Cellular Endocrinology, 2011
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