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pro vyhledávání: '"Karel Cutka"'
Autor:
Dominique Bonneau, Asbjørg Stray-Pedersen, Nathalie Biebuyck-Gouge, Georges Deschênes, Nihal Özdemir, Barbara Hinkelmann, Sandra Cockfield, Stavroula Psoni, Guiliana Lama, David V. Milford, Maria Kanariou, Helen Fryssira, Anja Stein, Lawrence R. Shoemaker, Silvia Majore, Sarah F. Smithson, Natasa Stajic, Isabel Cordeiro, Onur Sakallioglu, Belde Kasap, Helen Georgaki, Beate Schmidt, Valérie Cormier-Daire, Newton A C S Wong, Bertram F. Pontz, Radovan Bogdanovic, Flora Sotsiou, Encarna Guillén-Navarro, Doris Taha, Cornelius F. Boerkoel, Graham Smith, Sara Sebnem Kilic, Kunho Choi, Stefan Fründ, Karel Cutka, J. Marietta Clewing, Shu Lou, Petra Lamfers, Karlien Cransberg, Emily A. Sloan, Pierre Cochat, Yumi Asakura, Chantal Loirat, Jochen H. H. Ehrich, Denis Morin, Jane Tizard, Herbert Reichenbach, David Goodman, Michel Tsimaratos, Cristina Rusu, Laure Collard, Harika Alpay, Yan Huang, Jorge M. Saraiva, Sabine Sigaudy, Willem Proesmans, Thomas Lücke, Sophie Taque, Jean Luc André, Caterina Cancrini, Silke Reif
Schimke immunoosseous dysplasia (SIOD), which is characterized by prominent spondyloepiplayseal dysplasia, T-cell deficiency, and focal segmental glomerulosclerosis, is a panethnic autosomal recessive multisystem disorder with variable expressivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a509839dac6bcb390f642383f690409f
https://avesis.deu.edu.tr/publication/details/da3be966-7ee9-4d6f-a09b-18e79d6dbac2/oai
https://avesis.deu.edu.tr/publication/details/da3be966-7ee9-4d6f-a09b-18e79d6dbac2/oai