Browsing by Author Rauch, F

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Issue DateTitleAuthor(s)Citation
2015Homozygosity for Frameshift Mutations in XYLT2 Result in a Spondylo-Ocular Syndrome with Bone Fragility, Cataracts, and Hearing DefectsMunns, Craig; Sillence, David; Biggin, Andrew; Fahiminiya, Somayyeh; Fassier, Francois; Glorieux, Francis H; Hinsdale, Myron E; Majewski, Jacek; Metcalf, Jordan P; Munteanu, Maria Cristina; Poudel, Nabin; Rauch, F; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthHomozygosity for Frameshift Mutations in XYLT2 Result in a Spondylo-Ocular Syndrome with Bone Fragility, Cataracts, and Hearing Defects, American Journal of Human Genetics, vol.96, 6, 2015,pp 971-978
2008Scaling and adjusting growth-related data and sex-differences in the muscle-bone relation: a perspectiveCowell, Christopher; Blimkie, Cameron J. R.; Hoegler, W.; Rauch, F; Woodhead, H. J.; Children's Hospital Westmead: Paediatrics & Child HealthScaling and adjusting growth-related data and sex-differences in the muscle-bone relation: a perspective, Journal of Musculoskeletal and Neuronal Interactions, vol.8,(1),2008,pp 25-28
2008Sex-specific developmental changes in muscle size and bone geometry at the femoral shaftCowell, Christopher; Blimkie, Cameron J. R.; Farpour-Lambert, Nathalie; Holger, W; Inglis, D; Kemp, A F; Rauch, F; Wiebe, P; Woodhead, H. J.; Children's Hospital Westmead: Paediatrics & Child HealthSex-specific developmental changes in muscle size and bone geometry at the femoral shaft, Bone, vol.42, 5, 2008,pp 982-989