Today's Hours: 8:00am - 6:00pm

Search

Filter Applied Clear All

Did You Mean:

Search Results

  • Book
    volume editor, Richard Quinton.
    Contents:
    Molecular characterization and phenotypic expression of mutations in genes for gonadotropins and their receptors in humans / Salvi, R., Pralong, F.P
    Role of kisspeptin/GPR54 system in human reproductive axis / Silveira, L.F.G. ... [et al.]
    Biology of kisspeptins / Hameed, S., Dhillo, W.S.
    Role of fibroblast growth factor signaling in gonadotropin-releasing hormone neuronal system development / Chung, W.C.J., Tsai, P.-S.
    FGFR1 mutations in Kallmann syndrome / Villanueva, C., de Roux, N.
    Biology of KAL1 and its orthologs : implications for x-linked Kallmann syndrome and the search for novel candidate genes / MacColl, G.S., Quinton, R., Bülow, H.E.
    Biological actions and interactions of anosmin-1 / Choy, C., Kim, S.H.
    Genotype and phenotype of patients with gonadotropin-releasing hormone receptor mutations / Kim, H.-G. ... [et al.]
    Hypogonadotropic hypogonadism and GNRH1 mutations in mice and humans / Bouligand, J. ... [et al.]
    Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes : pathophysiology and genotype-phenotype correlations / Sarfati, J., Dodé, C., Young, J.
    Neurokinin B and its receptor in hypogonadotropic hypogonadism / Semple, R.K., Topaloglu, A.K.
    Complex genetics in idiopathic hypogonadotropic hypogonadism / Pitteloud, N. ... [et al.]
    Rarer syndromes characterized by hypogonadotropic hypogonadism / Aminzadeh, M. ... [et al.].
    Digital Access Karger 2010