Kallmann syndrome: fibroblast growth factor signaling insufficiency?

Author:

Dod� Catherine,Hardelin Jean-Pierre

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Drug Discovery,Molecular Medicine

Reference90 articles.

1. Hardelin J-P (2001) Kallmann syndrome: towards molecular pathogenesis. Mol Cell Endocrinol 179:75?81

2. Dodé C, Levilliers J, Dupont J-M et al. (2003) FGFR1 loss-of-function mutations cause autosomal dominant Kallmann syndrome. Nat Genet 33:463?465

3. Naftolin F, Harris GW, Bobrow M (1971) Effect of purified luteinizing hormone releasing factor on normal and hypogonadotropic anosmic men. Nature 232:496?497

4. Morsier G de (1954) Etudes sur les dysraphies crânio-encéphaliques. I. Agénésie des lobes olfactifs (telencephaloschizis latéral) et des commissures calleuse et antérieure (telencephaloschizis médian). La dysplasie olfacto-génitale. Schweiz Arch Neurol Psychiatry 74:309?361

5. Kallmann FJ, Schoenfeld WA, Barrera SE (1944) The genetic aspects of primary eunuchoidism. Am J Ment Defic 48:203?236

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