 | Up a level |
Øzdemir, Cagla Margit; Nielsen, Mette Mølby; Liimatta, Jani; Voegel, Clarissa D; Naamneh Elzenaty, Rawda; Wasehuus, Victor S; Lind-Holst, Marie; Ornstrup, Marie Juul; Gram, Stine Bjørn; Ousager, Lilian Bomme; Flück, Christa E; Gravholt, Claus H (2024). Late diagnosis of partial 3β-hydroxysteroid dehydrogenase type 2 deficiency - characterization of a new genetic variant. Endocrinology, diabetes & metabolism case reports, 2024(3) Bioscientifica 10.1530/EDM-23-0090
Burget, Lukas; Parera, Laura Audí; Fernandez-Cancio, Monica; Gräni, Rolf; Henzen, Christoph; Flück Pandey, Christa Emma (2018). A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the gene. Endocrinology, diabetes & metabolism case reports, 2018(1) Bioscientifica 10.1530/EDM-18-0003
Choy, John; Hofstetter, Wilhelm; Klenke, Frank M. (2013). RANKL immobilized on β-TCP induces and maintains osteoclast formation. Bone Abstracts, 1, PP227. Bioscientifica 10.1530/boneabs.1.PP227
