Reversible Congenital Hypogonadotropic Hypogonadism in Patients with CHD7, FGFR1 or GNRHR Mutations

por Laitinen, Eeva-Maria, Tommiska, Johanna, Sane, Timo, Vaaralahti, Kirsi, Toppari, Jorma, Raivio, Taneli
Publicado 2012

Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

por Laitinen, Eeva-Maria, Vaaralahti, Kirsi, Tommiska, Johanna, Eklund, Elina, Tervaniemi, Mari, Valanne, Leena, Raivio, Taneli
Publicado 2011