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kw.\*:("Gène KAL")

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Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndromeLEGOUIS, R; COHEN-SALMON, M; DEL CASTILLO, I et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 2, pp 516-518, issn 0888-7543Article

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndromeHARDELIN, J.-P; LEVILLIERS, J; BLANCHARD, S et al.Human molecular genetics (Print). 1993, Vol 2, Num 4, pp 373-377, issn 0964-6906Article

Molecular basis of the X-chromosome-linked Kallmann's syndromePETIT, C.Trends in endocrinology and metabolism. 1993, Vol 4, Num 1, pp 8-13, issn 1043-2760Article

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion moleculesLEGOUIS, R; HARDELIN, J.-P; LUTFALLA, G et al.Cell (Cambridge). 1991, Vol 67, Num 2, pp 423-435, issn 0092-8674Article

Expression of the KAL gene in multiple neuronal sites during chicken developmentLEGOUIS, R; AYER-LE LIEVRE, C; LEIBOVICI, M et al.Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 6, pp 2461-2465, issn 0027-8424Article

Etude structurale et fonctionnelle du gène responsable du syndrome de Kallmann lié au chromosome X et de son homologue sur le chromosome Y = Structural and fonctionnal study of the X-chromosome linked Kallmann syndrome gene, and its homologous gene on the Y chromosomeCohen-Salmon, Martine; Petit, C.1995, 201 p.Thesis

Kallmann's syndrome and schizophreniaVAGENAKIS, George A; HYPHANTIS, Thomas N; PAPAGEORGIOU, Charalabos et al.International journal of psychiatry in medicine. 2004, Vol 34, Num 4, pp 379-390, issn 0091-2174, 12 p.Article

Syndromes malformatifs rénaux chez l'homme : Ce qu'ils nous apprennent sur la différenciation du rein = Renal MalformationWOOLF, A. S; BEALES, P. L; FEATHER, S. A et al.Actualités néphrologiques Jean Hamburger. 1999, pp 276-285, issn 1168-1098Article

Genetics of hypogonadotropic hypogonadismSEMINARA, S. B; OLIVEIRA, L. M. B; BERANOVA, M et al.Journal of endocrinological investigation (Testo stampato). 2000, Vol 23, Num 9, pp 560-565, issn 0391-4097Article

Anomalies génétiques de l'axe gonadotrope = Genetic abnormalities of the gonadotropic axisDE ROUX, N; MOREL, Y; HARDELIN, J.-P et al.La Revue du praticien (Paris). 1999, Vol 49, Num 12, pp 1277-1282, issn 0035-2640Article

Renal abnormalities in patients with Kallmann syndromeZENTENO, J. C; MENDEZ, J. P; MAYA-NUNEZ, G et al.British journal of urology (Print). 1999, Vol 83, Num 4, pp 383-386, issn 0007-1331Article

Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patientsTRARBACH, Ericka B; BAPTISTA, Maria T. M; GARMES, Heraldo M et al.Journal of endocrinology. 2005, Vol 187, Num 3, pp 361-368, issn 0022-0795, 8 p.Article

Aménorrhées : génétique moléculaire = The molecular genetics of amenorrheaPARIS, F; LUMBROSO, S; SULTAN, C et al.Références en gynécologie obstétrique. 2001, Vol 8, Num 6, pp 497-505, issn 1244-8168Article

Neue Erkenntnisse zur Genetik des Kallmann-Syndroms und des Idiopathischen Hypogonadotropen Hypogonadismus (IHH) = New genetic aspects of Kallmann syndrome and idiopathic hypogonadotropic hypogonadism (IHH)MESCHEDE, D; HORST, J.Geburtshilfe und Frauenheilkunde. 1999, Vol 59, Num 8, pp 381-386, issn 0016-5751Article

X chromosome-linked Kallmann syndrome: Clinical heterogeneity in three siblings carrying an intragenic deletion of the KAL-1 geneMASSIN, Nathalie; PECHEUX, Christophe; ELOIT, Corinne et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 5, pp 2003-2008, issn 0021-972X, 6 p.Article

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