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Autor:
R M, Patel, S C S, Nagamani, D, Cuthbertson, P M, Campeau, J P, Krischer, J R, Shapiro, R D, Steiner, P A, Smith, M B, Bober, P H, Byers, M, Pepin, M, Durigova, F H, Glorieux, F, Rauch, B H, Lee, T, Hart, V R, Sutton
Publikováno v:
Clinical genetics. 87(2)
Osteogenesis imperfecta (OI) is the most common skeletal dysplasia that predisposes to recurrent fractures and bone deformities. In spite of significant advances in understanding the genetic basis of OI, there have been no large-scale natural history