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Mutations in <it>LRP5 </it>cause primary osteoporosis without features of OI by reducing Wnt signaling activity by Korvala Johanna, Jüppner Harald, Mäkitie Outi, Sochett Etienne, Schnabel Dirk, Mora Stefano, Bartels Cynthia F, Warman Matthew L, Deraska Donald, Cole William G, Hartikka Heini, Ala-Kokko Leena, Männikkö Minna
Published 2012-04-01
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Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid overdose by Corradin, Olivia, Sallari, Richard, Hoang, An T, Kassim, Bibi S, Ben Hutta, Gabriella, Cuoto, Lizette, Quach, Bryan C, Lovrenert, Katreya, Hays, Cameron, Gryder, Berkley E, Iskhakova, Marina, Cates, Hannah, Song, Yanwei, Bartels, Cynthia F, Hancock, Dana B, Mash, Deborah C, Johnson, Eric O, Akbarian, Schahram, Scacheri, Peter C
Published 2022
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