Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in FinlandEeva‐Maria Laitinen(Helsinki University Hospital), Taneli Raivio(University of Helsinki)Orphanet Journal of Rare DiseasesJune 17, 201110.1186/1750-1172-6-41Cited by 192SaveCiteExport RISWatch citationsRelated PapersTreatment of gonadotropin deficiency during the first year of life: long-term observation and outcome in five boys|Human Reproduction|2019|49GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiency|PLoS ONE|2017|22