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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1993
[Osteogenesis imperfecta in childhood and adolescence]R E Brenner, B Schiller, B F Pontz, et al.
Journal of Medical Genetics|April 5, 2005
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)K W Kjaer, L Hansen, G C Schwabe, et al.
American Journal of Medical Genetics|September 1, 1982
AtelosteogenesisP Maroteaux, J Spranger, V Stanescu, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 30, 2018
Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2S Butscheidt, A Delsmann, T Rolvien, et al.
Osteoarthritis and Cartilage|January 21, 2020
Skeletal deterioration in COL2A1-related spondyloepiphyseal dysplasia occurs prior to osteoarthritisT Rolvien, T A Yorgan, U Kornak, et al.
International Journal of Sports Medicine|January 21, 2012
Leptin and endocrine parameters in marathon runnersT Bobbert, K Mai, L Brechtel, et al.
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