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5. [Association between hypogonadotrophic hypogonadism and familial deafness: a variation of Kallmann's syndrome?]. Floret D; Philippe N; Boschetti R; Martin H; Monnet P J Genet Hum; 1976 Nov; 24 Suppl():207-14. PubMed ID: 1025272 [No Abstract] [Full Text] [Related]
6. Loss of function mutations of the GnRH receptor: a new cause of hypogonadotropic hypogonadism. de Roux N; Young J; Misrahi M; Schaison G; Milgrom E J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():267-75. PubMed ID: 10698591 [TBL] [Abstract][Full Text] [Related]
7. [Hypogonadotrophic hypogonadism and dysosmia]. Ubachs JM; Rolland R Ned Tijdschr Geneeskd; 1978 Dec; 122(49):1912-6. PubMed ID: 723977 [No Abstract] [Full Text] [Related]
8. Hypogonadotropic hypogonadism with anosmia (Kallmann's syndrome) unresponsive to clomiphene citrate. Schroffner WG; Furth ED J Clin Endocrinol Metab; 1970 Sep; 31(3):267-70. PubMed ID: 5453324 [No Abstract] [Full Text] [Related]
9. [Bilateral Duane syndrome associated with hypogonadotropic hypogonadism and anosmia (Kallmann syndrome)]. Cordonnier M; Hanozet V; Van Nechel C; Fery F; Aberkane J Bull Soc Belge Ophtalmol; 1990; 239():29-35. PubMed ID: 2133532 [TBL] [Abstract][Full Text] [Related]
10. Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations. Seminara SB; Hayes FJ; Crowley WF Endocr Rev; 1998 Oct; 19(5):521-39. PubMed ID: 9793755 [No Abstract] [Full Text] [Related]
11. Heterogeneity of Kallmann's syndrome. Hermanussen M; Sippell WG Clin Genet; 1985 Aug; 28(2):106-11. PubMed ID: 4042391 [TBL] [Abstract][Full Text] [Related]
12. [Kallmann's syndrome. Apropos of 2 personal cases]. Ponticelli C; Frosini P; Masi L Acta Otorhinolaryngol Ital; 1991; 11(6):603-8. PubMed ID: 1819188 [TBL] [Abstract][Full Text] [Related]
18. A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+). Ventruto V; Cali A; Farina L; Festa B; Ricciardi I; Sebastio L J Med Genet; 1976 Feb; 13(1):71-5. PubMed ID: 1271431 [TBL] [Abstract][Full Text] [Related]
19. A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism. Johnson VP; McMillin JM; Aceto T; Bruins G Am J Med Genet; 1983 Jul; 15(3):497-506. PubMed ID: 6881216 [TBL] [Abstract][Full Text] [Related]
20. [Familial hypogonadism with anosmia: Kallmann Syndrome]. Brämswig JH; Schellong G; König A; Stubbe P Monatsschr Kinderheilkd; 1983 Apr; 131(4):232-4. PubMed ID: 6865980 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]