References
- Schwarts CE, Dean J, Howard-Peebles PN, Bugge M, Mikkelsen M, Tommerup N, et al. Obstetrical and gynaecological complications in fragile X carriers: a multicenter study. Am J Med Genet 1994; 51: 400–2
- Turner G, Webb T, Wake S, Robinson H. Prevalence of fragile X syndrome. Am J Med Genet 1996; 64: 196–7
- Rousseau F, Rouillard P, Morel ML, Khandjian EW, Morgan K. Prevalence of carriers of premutation-size alleles of the FMR1 gene and implications for the population genetics of the fragile X syndrome. Am J Hum Genet 1995; 57: 1006–18
- Anasti JN. Premature ovarian failure: an update. Fertil Steril 1998; 70(1)1–15
- Oostra BA, Willemsen R. A fragile balance: FMR1 expression levels. Hum Mol Genet 2003; 12(2)249–57
- Welt CK, Smith PC, Taylor AE. Evidence of early aging in fragile X premutation carriers. J Clin Endocrinol Metab 2004; 89: 4569–74
- Allen EG, He W, Yadav-Shah M, Sherman SL. A study of the distributional characteristics of FMR1 transcript levels in 238 individuals. Hum Genet 2004; 114: 439–47
- Platteau P, Sermon K, Seneca S, Van Steirteghem A, Devroey P, Liebaers I. Preimplantation genetic diagnosis for fragile Xa syndrome; difficult but not impossible. Hum Reprod 2002; 17: 2807–12
- Laml T, Preyer O, Umek W, Hengstschlager M, Hanzal H. Genetic disorders in premature ovarian failure. Hum Reprod Update 2002; 8: 483–91