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Human Reproduction (Oxford, England)|December 12, 2017
New intronic Fibroblast Growth Factor Receptor 1 (FGFR1) mutation leading to disrupted splicing and Kallmann syndromeJ Känsäkoski, K Vaaralahti, T Raivio
International Journal of Andrology|January 18, 2012
Bone mineral density, body composition and bone turnover in patients with congenital hypogonadotropic hypogonadismE-M Laitinen, M Hero, K Vaaralahti, et al.
Molecular Syndromology|August 3, 2012
Genetic Overlap between Holoprosencephaly and Kallmann SyndromeK Vaaralahti, T Raivio, R Koivu, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 19, 2012
Cholesterol metabolism altered and FGF21 levels high after pediatric liver transplantation despite normal serum lipidsS Kosola, H Lampela, H Gylling, et al.
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