Giri, D; Bockenhauer, D; Deshpande, C; Achermann, JC; Taylor, NF; Rumsby, G; Morgan, H; ... Ajzensztejn, M; + view all (2020) Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations. Hormone Research in Paediatrics 10.1159/000507577. (In press). Green open access