1Hardelin JP, Levilliers J, Young J, et al. Xp22.3 Deletions in isolated familial Kallmann's syndrome[J]. J Clin Endoerinol Metab, 1993,76:827-831.
2Anna C,Federica P,Sophia C,et al. The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone(GnRH)-producing neuronsHum [J]. Molgenet, 2004,13(11 ) : 2 781-2 791.
3Naoko S, Noriyuki K, Masayo K, et al. Clinical Assessment and Mutation Analysis of Kallmann Syndrome 1 (KAL1)and Fibroblast Growth Factor Receptor 1 (FGFR1, or KAL2)in Five Families and 18 Sporadic Patients[J].J Clin Endocrinol Metab, 2004, 89:1 079-1 088313:2 781-2 791.
4Nelly Pitteloud, James S, Aciemo JR. Reversible Kallmann Syndrome, Delayed Puberty, and Isolated Anosmia Occurring in a Single Family with a Mutation in the Fibroblast Growth Factor Receptor 1 Gene[J]. J Clin Endocrinol Metab, 2005, 90:1 317- 1 322.
5史轶繁 主编.协和内分泌和代谢学[M].北京：科学出版社,2000.912-915.
6Buchter D, Behre HM, Kliesch S, et al. Pulsatile GnRH or human chorionic gonadotropin/human menopausal Kallmann's syndrome gonadotropin as effective treatment for men with hypogonadotropic hypogonadism:a review of 42 cases[J]. Eur J Endocrinol, 1998,139:298-303.
