Increased Burden of Common Risk Alleles in Children With a Significant Fracture History
ABSTRACT Extreme presentations of common disease in children are often presumed to be of Mendelian etiology, but their polygenic basis has not been fully explored. We tested whether children with significant fracture history and no osteogenesis imperfecta (OI) are at increased polygenic risk for fra...
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Veröffentlicht in: | Journal of bone and mineral research 2020-05, Vol.35 (5), p.875-882 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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