Browsing Centre for Endocrinology by Author "Jain, V"
Now showing items 1-3 of 3
-
46,XY Partial gonadal dysgenesis; diagnosis and long-term outcome at puberty
Cuccaro, RT; Hughes, I; Cools, M; van de Vijver, K; de Mendonca, BB; Domenice, S; Batista, RL; Dallago, RT; Gomes, NL; Costa, EF (2022) -
Gonadal morphology in 46,XY gonadal dysgenesis: I-DSD Registry-based study
Tadokoro-Cuccaro, R; Hughes, I; Cools, M; van de Vijver, K; de Mendonca, BB; Domenice, S; Batista, RL; Dallago, RT; Gomes, NL; Costa, EF (2022) -
Neonatal presentation of familial glucocorticoid deficiency resulting from a novel splice mutation in the melanocortin 2 receptor accessory protein
Jain, V; Metherell, LA; David, A; Sharma, R; Sharma, PK; Clark, AJL; Chan, LF (2011-12)