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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. [Genetic considerations on Kallmann's syndrome (hypogonadotropic hypogenitalism with anosmia)]. Juillard E Rev Med Suisse Romande; 1978 May; 98(5):237-41. PubMed ID: 663494 [No Abstract] [Full Text] [Related]
7. 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]
8. Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome. Bick D; Franco B; Sherins RJ; Heye B; Pike L; Crawford J; Maddalena A; Incerti B; Pragliola A; Meitinger T; Ballabio A N Engl J Med; 1992 Jun; 326(26):1752-5. PubMed ID: 1594017 [No Abstract] [Full Text] [Related]
9. Father-to-son transmission of hypogonadism with anosmia: Kallmann's syndrome. Merriam GR; Beitins IZ; Bode HH Am J Dis Child; 1977 Nov; 131(11):1216-9. PubMed ID: 335879 [TBL] [Abstract][Full Text] [Related]
10. Identical twins discordant for Kallmann's syndrome. Hipkin LJ; Casson IF; Davis JC J Med Genet; 1990 Mar; 27(3):198-9. PubMed ID: 2325096 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. [From gene to disease; hypogonatrophic hypogonadism and anosmia: Kallmann's syndrome]. Voorhoeve PG; Delemarre-van de Waal HA Ned Tijdschr Geneeskd; 2004 Jun; 148(23):1142-4. PubMed ID: 15211964 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Franco B; Guioli S; Pragliola A; Incerti B; Bardoni B; Tonlorenzi R; Carrozzo R; Maestrini E; Pieretti M; Taillon-Miller P; Brown CJ; Willard HF; Lawrence C; Graziella Persico M; Camerino G; Ballabio A Nature; 1991 Oct; 353(6344):529-36. PubMed ID: 1922361 [TBL] [Abstract][Full Text] [Related]
17. Isolated hypogonadotrophic hypogonadism: a family with autosomal dominant inheritance. Dean JC; Johnston AW; Klopper AI Clin Endocrinol (Oxf); 1990 Mar; 32(3):341-7. PubMed ID: 2111748 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Diagnosis of Kallmann's syndrome in early infancy. Evain-Brion D; Gendrel D; Bozzola M; Chaussain JL; Job JC Acta Paediatr Scand; 1982 Nov; 71(6):937-40. PubMed ID: 6984277 [No Abstract] [Full Text] [Related] [Next] [New Search]