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pro vyhledávání: '"Heidi, Oehlandt"'
Autor:
Jorma Toppari, Kirsi Vaaralahti, Johanna Tommiska, Helena E. Virtanen, Heidi Oehlandt, Rosanna Koivu, Taneli Raivio, Eeva-Maria Laitinen
Publikováno v:
Molecular and Cellular Endocrinology
Molecular and Cellular Endocrinology, Elsevier, 2011, 341 (1-2), pp.35. ⟨10.1016/j.mce.2011.05.015⟩
Molecular and Cellular Endocrinology, Elsevier, 2011, 341 (1-2), pp.35. ⟨10.1016/j.mce.2011.05.015⟩
Mutations in FGFR1 , GNRHR , PROK2 , PROKR2 , TAC3 , or TACR3 underlie isolated hypogonadotropic hypogonadism (IHH) with clinically variable phenotypes, and, by causing incomplete intrauterine activation of the hypothalamic–pituitary–gonadal axis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb55faac50bfc21d563c745856215f26
https://hal.archives-ouvertes.fr/hal-00719875/document
https://hal.archives-ouvertes.fr/hal-00719875/document