卵巢早衰相关的遗传学研究进展(3)
[8]Allen EG, Sullivan AK, Marcus M, et al. Examination of reproductive aging milestones among women who carry the FMR1 premutation[J]. Hum Reprod, 2007, 22(8):2142-2152.
[9]Murray A, Webb J, Dennis N, et al. Microdeletions in FMR2 may be a signi?cant cause of premature ovarian failure[J]. J Med Genet,1999,36(10):767-770.
[10]Conway GS，Payne NN，Webb J，et al.Fragile X permutation screening in women with premature ovarian failure[J].Hum Reprod，1998,13:1184-1187.
[11]Aaltonen J，Laitinen MP，Vuojolainen K，et al.Human growth differentiation factor 9(GDF-9) and its novel homolog GDF-9B are expressed in oocytes during early folliculogenesis[J].J Clin Endocrinol Metab, 1999，84(8)：2744-2750.
[12]Ledig S，Ropke A，Haeusler G，et al.Bmpl5 mutations in XX gonadal dysqenesis and premature ovarian failure[J]. Am J Obstet Gyneco，2008, 198(1):84-85.
[13]Aittomaki K，Lucena JL, Pakarinen P，et al.Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure[J].Cell,1995,82：959-968.
[14]陈新娜，陈贵安，李美芝.卵巢早衰患者卵泡刺激素受体基因突变的检测[J].中华妇产科杂志，2006，41(5)：315-318.
[15]Menon KM，Munshi UM，Clouser CL，et al.Regulation of luteinizing hormone/human ehorionie gonadotropin receptor expression:a perspectivel[J].Biol Reprod，2004，70(4)：861-866.
[16]Crisponi L，Deiana M，Loi A，et al.The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome[J].Nat Genet，2001，27(2)：159-166.
[17]Shelling AN，Burton KA，Chand AL，et al.Lnhibin：a candidate gene for premature ovarian failure[J].Hum Reprod,2000,15(12): 2644-2649.
(收稿日期：2012-03-19), 百拇医药(洪芳，丘彦)
[9]Murray A, Webb J, Dennis N, et al. Microdeletions in FMR2 may be a signi?cant cause of premature ovarian failure[J]. J Med Genet,1999,36(10):767-770.
[10]Conway GS，Payne NN，Webb J，et al.Fragile X permutation screening in women with premature ovarian failure[J].Hum Reprod，1998,13:1184-1187.
[11]Aaltonen J，Laitinen MP，Vuojolainen K，et al.Human growth differentiation factor 9(GDF-9) and its novel homolog GDF-9B are expressed in oocytes during early folliculogenesis[J].J Clin Endocrinol Metab, 1999，84(8)：2744-2750.
[12]Ledig S，Ropke A，Haeusler G，et al.Bmpl5 mutations in XX gonadal dysqenesis and premature ovarian failure[J]. Am J Obstet Gyneco，2008, 198(1):84-85.
[13]Aittomaki K，Lucena JL, Pakarinen P，et al.Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure[J].Cell,1995,82：959-968.
[14]陈新娜，陈贵安，李美芝.卵巢早衰患者卵泡刺激素受体基因突变的检测[J].中华妇产科杂志，2006，41(5)：315-318.
[15]Menon KM，Munshi UM，Clouser CL，et al.Regulation of luteinizing hormone/human ehorionie gonadotropin receptor expression:a perspectivel[J].Biol Reprod，2004，70(4)：861-866.
[16]Crisponi L，Deiana M，Loi A，et al.The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome[J].Nat Genet，2001，27(2)：159-166.
[17]Shelling AN，Burton KA，Chand AL，et al.Lnhibin：a candidate gene for premature ovarian failure[J].Hum Reprod,2000,15(12): 2644-2649.
(收稿日期：2012-03-19), 百拇医药(洪芳，丘彦)