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pro vyhledávání: '"Kirsi Vaaralahti"'
Autor:
Taneli Raivio, Kirsi Vaaralahti, R. Koivu, Eeva-Maria Laitinen, Johanna Tommiska, Leena Valanne
Publikováno v:
Europe PubMed Central
Patients with Kallmann syndrome (KS; congenital hypogonadotropic hypogonadism and decreased/absent sense of smell), septo-optic dysplasia (SOD), or holoprosencephaly (HPE) reportedly have midline defects. In this study, we investigate a genetic overl