Accès gratuit
Med Sci (Paris)
Volume 19, Numéro 10, Octobre 2003
Page(s) 950 - 954
Section M/S Revues
Publié en ligne 15 octobre 2003
  1. Koenig M, Hoffman EP, Bertelson CJ, et al. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 1987; 50: 509–17.
  2. Kerem B, Rommens JM, Buchanan JA, et al. Identification of the cystic fibrosis gene: genetic analysis. Science 1989; 245: 1073–80.
  3. Oberle I, Rousseau F, Heitz D, et al. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science 1991; 252: 1097–102.
  4. A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group. Science 1992; 258: 67–86.
  5. Donis-Keller H, Green P, Helms C, et al. A genetic linkage map of the human genome. Cell 1987; 51: 319–37.
  6. Dib C, Faure S, Fizames C, et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996; 380: 152–4.
  7. Lander ES, Linton LM, Birren B, et al. Initial sequencing and analysis of the human genome. Nature 2001; 409: 860–921.
  8. Venter JC, Adams MD, Myers EW, et al. The sequence of the human genome. Science 2001; 291: 1304–51.
  9. Rao DC. Genetic dissection of complex traits: an overview. Adv Genet 2001; 42: 13–34.
  10. Giguere Y, Rousseau F. The genetics of osteoporosis: complexities and difficulties. Clin Genet 2000; 57: 161–9.
  11. Giguere Y, Dodin S, Blanchet C, et al. The association between heel ultrasound and hormone replacement therapy is modulated by a two-locus vitamin D and estrogen receptor genotype. J Bone Miner Res 2000; 15: 1076–84.
  12. Giguere Y, Dewailly E, Brisson J, et al. Short polyglutamine tracts in the androgen receptor are protective against breast cancer in the general population. Cancer Res 2001; 61: 5869–74.
  13. Thompson G. Significance levels in genome scans. Adv Genet 2001; 42: 475–86.
  14. Ponder B. Cancer genetics. Nature 2001; 411: 336–95.
  15. Kirk KM, Cardon LR. The impact of genotyping error on haplotype reconstruction and frequency estimation. Eur J Hum Genet 2002; 10: 616–22.
  16. Morton NE, Collins A. Tests and estimates of allelic association in complex inheritance. Proc Natl Acad Sci USA 1998; 95: 11389–93.
  17. Cardon L, Bell J. Association studies designs for complex diseases. Nat Rev Genet 2001; 2: 91–9.
  18. Longmate J. Complexity and power in case-control association studies. Am J Hum Genet 2001; 68: 1229–37.
  19. Hoh J, Wille A, Ott J. Trimming, weighting, and grouping SNPs in human case-control association studies. Genome Res 2001; 11: 2115–9.
  20. Xu J, Turner A, Little J, et al. Positive results in association studies are associated with departure from Hardy-Weinberg equilibrium: hint for genotyping error ? Hum Genet 2002; 111: 573–4.
  21. Committee on DNA-Diagnostics. DNA Diagnostics. Rijswijk: Health Council of the Netherlands, 1998.
  22. Rousseau F, Rouillard P, Morel ML, et al. Prevalence of carriers of premutationsize alleles of the FMRI gene and implications for the population genetics of the fragile X syndrome. Am J Hum Genet 1995; 57: 1006–18.
  23. Dombrowski C, Levesque S, Morel ML, et al. Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles. Hum Mol Genet 2002; 11: 371–8.
  24. Girouard J, Giguère Y, Delage R, et al. Prevalence of HFE gene C282Y and H63D mutations in a French-Canadian population of neonates and in referred patients. Hum Mol Genet 2002; 11: 185–9.

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