07 Jun 2013
A study from the US and Brazil published in The New England Journal of Medicine and to be presented at ENDO 2013 identifies loss of function mutations in a single gene in several families displaying a history of central precocious puberty. Further analysis suggests that in all affected individuals included in the study, the mutated gene was inherited from the father.
Call for nominations for Awards Committee Chair
30 Oct 2024
James M Tanner Award - 2025 nominations open
30 Oct 2024
Would you like to host the BSPED annual meeting?
21 Oct 2024