Associated Papers
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.
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Whole-Exome Sequencing Revealed New Candidate Genes for Human Dilated Cardiomyopathy.
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Diagnostics (basel, Switzerland), 2022
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Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency.
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Embo Molecular Medicine, 2016
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