Homozygosity mapping in family segregating premature ovarian insufficiency (POI)

ChEBI2014-03-20 更新2026-07-21 收录

遗传病基因定位

早发性卵巢功能不全

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Homozygosity mapping in family segregating premature ovarian insufficiency (POI)

创建时间：

2014-03-20

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Identify urinary exosome microRNAs that are unique to premature ovarian insufficiency. Identify urinary exosome microRNAs that are unique to premature ovarian insufficiency

早发性卵巢功能不全

外泌体miRNA分析

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NIAID Data Ecosystem40

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早发性卵巢功能不全

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DataCite Commons2025-04-26 更新70

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家畜基因组学

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NIAID Data Ecosystem40