Free Access
Issue
Med Sci (Paris)
Volume 21, Number 11, Novembre 2005
Page(s) 987 - 992
Section M/S revues
DOI https://doi.org/10.1051/medsci/20052111987
Published online 15 November 2005
  1. Jones KW, Singh L, Edwards RG. The use of probes for the Y chromosome in preimplantation embryo cells. Hum Reprod 1987; 2 : 439–45. [Google Scholar]
  2. Handyside AH, Lesko JG, Tarin JJ, et al. Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis. N Engl J Med 1992; 327 : 905–9. [Google Scholar]
  3. Geraedts J, Handyside A, Harper J, et al. ESHRE Preimplantation genetic diagnosis (PGD) Consortium : preliminary assessment of data from January 1997 to September 1998. ESHRE PGD Consortium steering committee. Hum Reprod 1999; 14 : 3138–48. [Google Scholar]
  4. Geraedts J, Handyside A, Harper J, et al. European society of human reproduction and embryology preimplantation genetic diagnosis consortium steering committee. ESHRE preimplantation genetic diagnosis (PGD) consortium : data collection II (May 2000). Hum Reprod 2000; 15 : 2673–83. [Google Scholar]
  5. ESHRE PGD Consortium steering committee. ESHRE Preimplantation genetic diagnosis consortium : data collection III (May 2001). Hum Reprod 2002; 17 : 233–46. [Google Scholar]
  6. Sermon K, Moutou C, Harper J, et al. ESHRE PGD Consortium data collection IV : May-December 2001. Hum Reprod 2005; 20 : 19–34. [Google Scholar]
  7. Handyside AH, Robinson MD, Simpson RJ, et al. Isothermal whole genome amplification from single and small numbers of cells : a new era for preimplantation genetic diagnosis of inherited disease. Mol Hum Reprod 2004; 10 : 767–72. [Google Scholar]
  8. Hellani A, Coskun S, Benkhalifa M, et al. Multiple displacement amplification on single cell and possible PGD applications. Mol Hum Reprod 2004; 10 : 847–52. [Google Scholar]
  9. Ray PF, Gigarel N, Bonnefont JP, et al. First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency. Prenat Diagn 2000; 20 : 1048–54. [Google Scholar]
  10. Gigarel N, Frydman N, Burlet P, et al. Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus, and incontinentia pigmenti loci on Xq28. Hum Genet 2004; 114 : 298–305. [Google Scholar]
  11. Gigarel N, Ray PF, Burlet P, et al. Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR. Mol Genet Metab 2005; 84 : 289–92. [Google Scholar]
  12. Steffann J, Frydman N, Gigarel N, et al. Analysis of mtDNA variant segregation during early human embryonic development : a tool for successful NARP preimplantation diagnosis. J Med Genet 2005 (online). [Google Scholar]
  13. Ray PF, Handyside AH. Increasing the denaturation temperature during the first cycles of amplification reduces allele dropout from single cells for preimplantation genetic diagnosis. Mol Hum Reprod 1996; 2 : 213–8. [Google Scholar]
  14. Ray PF, Munnich A, Nisand I, et al. The place of “social sexing” in medicine and science. Hum Reprod 2002; 17 : 248–9. [Google Scholar]
  15. Munne S, Chen S, Fischer J, et al. Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages. Fertil Steril 2005; 84 : 331–5. [Google Scholar]
  16. Platteau P, Staessen C, Michiels A, et al. Preimplantation genetic diagnosis for aneuploidy screening in women older than 37 years. Fertil Steril 2005; 84 : 319–24. [Google Scholar]
  17. Staessen C, Platteau P, Van Assche E, et al. Comparison of blastocyst transfer with or without preimplantation genetic diagnosis for aneuploidy screening in couples with advanced maternal age : a prospective randomized controlled trial. Hum Reprod 2004; 19 : 2849–58. [Google Scholar]
  18. Verlinsky Y, Rechitsky S, Schoolcraft W, et al. Preimplantation diagnosis for Fanconi anemia combined with HLA matching. JAMA 2001; 285 : 3130–3. [Google Scholar]
  19. Verlinsky Y, Rechitsky S, Sharapova T, et al. Preimplantation HLA testing. JAMA 2004; 291 : 2079–85. [Google Scholar]
  20. Ao A, Wells D, Handyside AH, et al. Preimplantation genetic diagnosis of inherited cancer : familial adenomatous polyposis coli. J Assist Reprod Genet 1998; 15 : 140–4. [Google Scholar]
  21. Simpson JL, Carson SA, Cisneros P. Preimplantation genetic diagnosis (PGD) for heritable neoplasia. J Natl Cancer Inst Monogr 2005; 34 : 87–90. [Google Scholar]
  22. Rechitsky S, Verlinsky O, Chistokhina A, et al. Preimplantation genetic diagnosis for cancer predisposition. Reprod Biomed Online 2002; 5 : 148–55. [Google Scholar]
  23. Verlinsky Y, Rechitsky S, Verlinsky O, et al. Preimplantation diagnosis for early-onset Alzheimer disease caused by V717L mutation. JAMA 2002; 287 : 1018–21. [Google Scholar]

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