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- Text 8
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Autor/in
- Amling, Michael
- Kornak, Uwe
- Schinke, Thorsten
- Oheim, Ralf 7
- Rolvien, Tim 7
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8 Einträge gefunden
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Clinical Phenotype and Relevance of LRP5 and LRP6 Variants in Patients With Early-Onset Osteoporosis (EOOP)
- Stürznickel, Julian
- Rolvien, Tim
- Delsmann, Alena
- Butscheidt, Sebastian
- Barvencik, Florian
- Mundlos, Stefan
- Schinke, Thorsten
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Compound heterozygous frameshift mutations in MESD cause a lethal syndrome suggestive of osteogenesis imperfecta type XX
- Stürznickel, Julian
- Jähn-Rickert, Katharina
- Zustin, Jozef
- Hennig, Floriane
- Delsmann, Maximilian M
- Schoner, Katharina
- Rehder, Helga
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Mice lacking plastin-3 display a specific defect of cortical bone acquisition
- Yorgan, Timur
- Sari, Hatice
- Rolvien, Tim
- Windhorst, Sabine
- Failla, Antonio Virgilio
- Kornak, Uwe
- Oheim, Ralf
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Clinical Significance of DXA and HR-pQCT in Autosomal Dominant Osteopetrosis (ADO II)
- Butscheidt, Sebastian
- Rolvien, Tim
- Kornak, Uwe
- Schmidt, Felix N
- Schinke, Thorsten
- Amling, Michael
- Oheim, Ralf
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A Novel ANO5 Mutation Causing Gnathodiaphyseal Dysplasia With High Bone Turnover Osteosclerosis
- Rolvien, Tim
- Koehne, Till
- Kornak, Uwe
- Lehmann, Wolfgang
- Amling, Michael
- Schinke, Thorsten
- Oheim, Ralf