Associated Papers
NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights.
Jordan P et al.
Journal of Assisted Reproduction and Genetics, 2024
Genomic Landscape of Normal and Breast Cancer Tissues in a Hungarian Pilot Cohort.
Pipek O et al.
International Journal of Molecular Sciences, 2023
37239898 (PubMed )
Supplement: ijms-24-08553-s001.zip › Supp_Fig_1_new.pdf
NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.
Bouali N et al.
Clinical Genetics, 2016
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