7Shekhar S.Familial normosmic idiopathic hypogonadotropic hypogonadism:is there a phenotypic marker for each genetic mutation? report of three cases and review of literature[J].BMJ Case Rep,2012:2012.
8Bouvattier C,Maione L,Bouligand J,et al.Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism[J].Nat Rev Endocrinol,2011,8:172-182.
9Pitteloud N,Meysing A,Quinton R,et al.Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes[J].Mol Cell Endocrinol,2006,254-255:60-69.
10Custer J,Rau R.The Harriet Lane handbook,18th ed,Endocrinology,Volume[M].Copyright Elsevier,2009.