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Number of items: 5.

Journal Article

Hoyer-Kuhn, H., Franklin, J., Allo, G., Kron, M., Netzer, C., Eysel, P., Hero, B., Schoenau, E. and Semler, O. (2016). Safety and efficacy of denosumab in children with osteogenesis imperfecta - a first prospective trial. J. Musculoskelet. Neuronal Interact., 16 (1). S. 24 - 33. NAFPLION: JMNI. ISSN 1108-7161

Lehnen, H., Schwennicke, G., Maiwald, R., Kunstmann, E., Kaiser, F. and Netzer, C. (2016). Prenatal Diagnosis - sonographic Abnormalities in two Pregnancies of a Family with a fetal renal tubular Dysgenesis and a Cornelia de Lange Syndrome. Geburtshilfe Frauenheilkd., 76 (5). STUTTGART: GEORG THIEME VERLAG KG. ISSN 1438-8804

Moosa, S., Chung, B. H. -Y., Tung, J. Y. -L., Altmueller, J., Thiele, H., Nuernberg, P., Netzer, C., Nishimura, G. and Wollnik, B. (2016). Mutations in SEC24D cause autosomal recessive osteogenesis imperfecta. Clin. Genet., 89 (4). S. 517 - 520. HOBOKEN: WILEY-BLACKWELL. ISSN 1399-0004

Moosa, S., Yamamoto, G. L., Garbes, L., Keupp, K., Beleza-Meireles, A., Moreno, C. A., Valadares, E. R., de Sousa, S. B., Maia, S., Saraiva, J., Honjo, R. S., Kim, C. A., Cabral de Menezes, H., Lausch, E., Lorini, P. V., Lamounier, A., Jr., Carniero, T. C. B., Giunta, C., Rohrbach, M., Janner, M., Semler, O., Beleggia, F., Li, Y., Yigit, G., Reintjes, N., Altmuller, J., Nurnberg, P., Cavalcanti, D. P., Zabel, B., Warman, M. L., Bertola, D. R., Wollnik, B. and Netzer, C. (2020). Severe Osteogenesis imperfecta with oligodontia: think of MESD. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 248 - 250. LONDON: SPRINGERNATURE. ISSN 1476-5438

Velmans, C., O'Donnell-Luria, A., Argilli, E., Tran-Mau-Them, F., Vitobello, A., Rech, M., Abicht, A., Aubert-Mucca, M., Carmichael, J., Chassaing, N., Clark, R., Coubes, C., de Dios, K., Funalot, B., Joseph, M., Kenendy, C., van de Laar, I., Lehalle, D., Leppig, K., Lessmeier, L., Pais, L., Paterson, H., Ramanathan, S., Sherr, E., Netzer, C., Schaaf, C. and Erger, F. (2020). Refining the phenotypic & mutational spectrum in a multinational cohort of O'Donnell-Luria-Rodan Syndrome. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 347 - 349. LONDON: SPRINGERNATURE. ISSN 1476-5438

This list was generated on Mon Mar 1 03:13:00 2021 CET.