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Early childhood exposures in relation to fragile X-associated primary ovarian insufficiency (FXPOI)
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Identification of Modifying Genes Associated with Fragile X Disorders Using TWAS
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Maximizing the ability to detect modifying genetic factors of rare complex disorders – Fragile X-Associated Primary Ovarian Insufficiency and Down Syndrome - Congenital Heart Defects
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Genome-wide transcriptome analysis in Fragile X-associated Primary Ovarian Insufficiency (FXPOI) disease
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