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- 2010006846 contributor B11744756.
- 2010006846 created "c2010.".
- 2010006846 date "2010".
- 2010006846 date "c2010.".
- 2010006846 dateCopyrighted "c2010.".
- 2010006846 description "Includes bibliographical references and indexes.".
- 2010006846 description "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.].".
- 2010006846 extent "x, 174 p. :".
- 2010006846 identifier "3805586175".
- 2010006846 identifier "9783805586177 (hc : alk. paper)".
- 2010006846 isPartOf "Frontiers of hormone research ; v. 39.".
- 2010006846 isPartOf "Frontiers of hormone research, 0301-3073 ; v. 39".
- 2010006846 issued "2010".
- 2010006846 issued "c2010.".
- 2010006846 language "eng".
- 2010006846 publisher "Basel [Switzerland] ; New York : Karger,".
- 2010006846 subject "616.4/7 22".
- 2010006846 subject "Hypogonadism genetics.".
- 2010006846 subject "Hypogonadism.".
- 2010006846 subject "Kallmann Syndrome genetics.".
- 2010006846 subject "RC898 .K35 2010".
- 2010006846 subject "W1 FR946F v.39 2010".
- 2010006846 subject "WK 900 K14 2010".
- 2010006846 tableOfContents "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.].".
- 2010006846 title "Kallmann syndrome and hypogonadotropic hypogonadism / volume editor, Richard Quinton.".
- 2010006846 type "text".