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Search Results - Roetzer, K.M.
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Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization
by
Roetzer, K.M.
,
Uyanik, G.
,
Brehm, A.
,
Zwerina, J.
,
Zandieh, S.
,
Czech, T.
,
Roschger, P.
,
Misof, B.M.
,
Klaushofer, K.
Published in
Bone (New York, N.Y.)
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Novel mutation in the carboxyl-terminal propeptide of the procollagen α1(I) chain in a girl with prenatal cortical hyperostosis and multiple fractures
by
Roetzer, K.M
,
Laccone, F
,
Krebs, A
,
Grill, F
,
Robins, S
,
Varga, F
,
Klaushofer, K
,
Al Kaissi, A
Published in
Bone (New York, N.Y.)
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Bone
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Bone Density - Genetics
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Bone Mineralization Density Distribution
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Cortical Bone
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Endocrinology & Metabolism
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Female
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Humans
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Life Sciences & Biomedicine
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Low Density Lipoprotein Receptor-Related Protein-5 - Genetics
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Lrp5 High Bone Mass Disorder
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Middle Aged
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Mutation
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Orthopedics
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Pedigree
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Quantitative Backscatter Electron Imaging
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Elsevier Sciencedirect Journals
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