A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism

por Fadiga, Lúcia, Lavrador, Mariana, Vicente, Nuno, Barros, Luísa, Gonçalves, Catarina I., Al-Naama, Asma, Saraiva, Luis R., Lemos, Manuel C.
Publicado 2022