X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.

Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. This syndrome is from a defect in the embryonic migratory pathway of gonadotropin-releasing hormone synthesizing neurons and olfactory axons. A candidate gene for the X chromosome-linked form of the syndrome...

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Bibliografske podrobnosti
Main Authors: Hardelin, J P, Levilliers, J, del Castillo, I, Cohen-Salmon, M, Legouis, R, Blanchard, S, Compain, S, Bouloux, P, Kirk, J, Moraine, C
Format: Artigo
Jezik:Inglês
Izdano: 1992
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC49883/
https://ncbi.nlm.nih.gov/pubmed/1518845
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