Associated Papers
Identification of novel variants underlying non-syndromic primary ovarian insufficiency using a targeted NGS gene panel.
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Frontiers in Endocrinology, 2025
41458559 (PubMed )
Supplement: Table4.xlsx › sheet1
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
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Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLRBS16_het
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