1Vegetti W, Marozzi A, Manfredini E, et al. Premature Ovarian Failure. Mol Cell Endocrinol, 2000,161(1-2):53-57
2Kalantaridou SN, Nelson LM. Premature ovarian failure is not premature menopause. Ann N Y Acad Sci, 2000,900:393-402
3Murray A. Premature ovarian failure and the FMR1 gene. Semin Reprod Med, 2000,18(1):59-66
4Marozzi A, Manfrodini E, Tibiletti MG, et al. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure. Hum Genet, 2000,107(4):304-311
5Davis CJ, Davison RM, Payne NN, et al. Female sex preponderance for idiopathic familial premature ovarian failure suggests an X chromosome defect:opinion. Hum Reprod, 2000,15(11):2418-2422
6Prueitt RL, Ross JL, Zinn AR. Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene. Cytogenet Cell Genet, 2000, 89(1-2):44-50
7Marozzi A, Vegetti W, Manfredini E, et al. Association between idiopathic premature ovarian failure and fragile X prematation. Hum Reprod, 2000,15(1):197-202
8Murray A, Webb J, MacSwiney F, et al. Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women. Hum Reprod,1999,14(5):1217-1218
9Hundscheid RD, Sistermans EA,Thomas CM ,et al. Imprinting effect in premature ovarian failure Confined to paternally inherited fragile X premutations. Am J Hum Genet,2000,66(2):413-418
10Hundscheid RD, Braat DD, kiemeney LA, et al. Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives. Hum Reprod,2001,16(3): 457-462
9Aittomaki K, Lucena JL, Pakarinen P, et al. Mutation in the follicle stimuLating hormone receptor gene causes hereditary hypergonadotropic ovarian failurel [J]. Cell, 1995,82:9592.
10Breidenbach M, Rein DT, Wang M, et al. Genetic replacement of the adenoviros shaft fiber reduces liver tropism in ovaran cancer gene therapy[ J ]. Hum Gene Ther,2004,15 : 509.
