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25. Kallmann syndrome associated with choanal atresia. Klein VR; Friedman JM; Brookshire GS; Brown OE; Edman CD Clin Genet; 1987 Apr; 31(4):224-7. PubMed ID: 3594930 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. A female case of Kallmann's syndrome. Iba K; Hamada N; Sowa E; Morii H; Wada M; Shiode S; Tanaka B; Hamada K Endocrinol Jpn; 1977 Aug; 23(4):289-93. PubMed ID: 336354 [TBL] [Abstract][Full Text] [Related]
28. Magnetic resonance imaging of the hypoplasia of the rhinencephalon in a patient with Kallmann's syndrome. Takeda T; Takasu N; Yamauchi K; Komiya I; Ohtsuka H; Nagasawa Y; Ohara N; Yamada T Intern Med; 1992 Mar; 31(3):394-6. PubMed ID: 1611194 [TBL] [Abstract][Full Text] [Related]
29. 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]
40. 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] [Previous] [Next] [New Search]