Associated Papers
The landscape of genetic variations in non-syndromic primary ovarian insufficiency in the MENA region: a systematic review.
Allouch A et al.
Frontiers in Endocrinology, 2023
NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.
Bouali N et al.
Clinical Genetics, 2016
Single nucleotide polymorphisms in premature ovarian failure-associated genes in a Chinese Hui population.
Ma L et al.
Molecular Medicine Reports, 2015
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