Hypogonadisme hypogonadotrope congénital = Congenital hypogonadotropic hypogonadismROZE, C; TOURAINE, P; LEGER, J et al.Annales d'endocrinologie. 2009, Vol 70, Num 1, pp 2-13, issn 0003-4266, 12 p.Article

A case of Kallmann syndrome associated with Dandy-Walker malformationUENO, H; YAMAGUCHI, H; KATAKAMI, H et al.Experimental and clinical endocrinology & diabetes. 2004, Vol 112, Num 1, pp 62-67, issn 0947-7349, 6 p.Article

Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndromeLEROY, Chrystel; FOUVEAUT, Corinne; LECLERCQ, Sandrine et al.European journal of human genetics. 2008, Vol 16, Num 7, pp 865-868, issn 1018-4813, 4 p.Article

Le syndrome de Kallmann de Morsier : génétique et physiopathologie = Kallmann de Morsier syndrome : genetics and pathophysiologyDODE, Catherine; TEIXEIRA, Luis; HARDELIN, Jean-Pierre et al.MT médecine de la reproduction gynécologie endocrinologie. 2008, Vol 10, Num 2, pp 131-134, 4 p.Article

Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndromeGEORGOPOULOS, Neoklis A; KOIKA, Vasiliki; KOUROUNIS, George et al.Fertility and sterility. 2007, Vol 88, Num 5, pp 1311-1317, issn 0015-0282, 7 p.Article

Kallmann Syndrome 1 Gene Is Expressed in the Marsupial GonadYANQIU HU; HONGSHI YU; SHAW, Geoff et al.Biology of reproduction. 2011, Vol 84, Num 3, pp 595-603, issn 0006-3363, 9 p.Article

Clinical genetics of Kallmann syndromeDODE, C; HARDELIN, J.-P.Annales d'endocrinologie. 2010, Vol 71, Num 3, pp 149-157, issn 0003-4266, 9 p.Conference Paper

Kallmann syndromeDODE, Catherine; HARDELIN, Jean-Pierre.European journal of human genetics. 2009, Vol 17, Num 2, pp 139-146, issn 1018-4813, 8 p.Article

A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3)BOULOUX, P.-M. G; HARDELIN, J.-P; MUNROE, P et al.Nucleic acids research. 1991, Vol 19, Num 19, issn 0305-1048, p. 5453Article

Identification of three novel mutations in the KAL1 gene in patients with Kallmann syndrome : The impact of the human genome on endocrinology: Special featuresSÖDERLUND, D; CANTO, P; MENDEZ, J. P et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 6, pp 2589-2592, issn 0021-972XArticle

Syndrome de Kallmann de Morsier : insuffisance de signalisation par les FGF ? = FGF-signaling insufficiency in Kallmann syndromeDODE, Catherine; HARDELIN, Jean-Pierre.MS. Médecine sciences. 2004, Vol 20, Num 8-9, pp 793-798, issn 0767-0974, 6 p.Article