Gonadotropin-Releasing Hormone Deficiency, Congenital Isolated
暂无分享,去创建一个
[1] J. Hardelin. Kallmann syndrome: towards molecular pathogenesis , 2001, Molecular and Cellular Endocrinology.
[2] W. Crowley,et al. The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. , 2001, The Journal of clinical endocrinology and metabolism.
[3] P. McDonough,et al. Mutations of follicle stimulating hormone-β and its receptor in human and mouse: genotype/phenotype , 2000, Molecular and Cellular Endocrinology.
[4] L. Layman. Genetics of human hypogonadotropic hypogonadism. , 1999, American journal of medical genetics.
[5] L. Layman. The molecular basis of human hypogonadotropic hypogonadism. , 1999, Molecular genetics and metabolism.
[6] J. Jameson,et al. Fertility and infertility: genetic contributions from the hypothalamic-pituitary-gonadal axis. , 1999, Molecular endocrinology.
[7] R. Fletterick,et al. DAX1 mutations map to putative structural domains in a deduced three-dimensional model. , 1998, American journal of human genetics.
[8] E. Rugarli,et al. Kallmann Syndrome: From Genetics to Neurobiology , 1993 .
[9] D. Bick,et al. Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism , 1998, Nature Genetics.
[10] J. Seidman,et al. Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency. , 1997, The Journal of clinical endocrinology and metabolism.