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BioMed Research International
Volume 2013 (2013), Article ID 585106, 9 pages
http://dx.doi.org/10.1155/2013/585106
Methodology Report

Novel One-Step Multiplex PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of -Thalassemia

1Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Avenida Manuel Siurot, s/n, 41013 Seville, Spain
2Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain

Received 4 February 2013; Revised 14 March 2013; Accepted 14 March 2013

Academic Editor: Thomas Liehr

Copyright © 2013 Raquel M. Fernández et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. T. N. Williams and D. J. Weatherall, “World distribution, population genetics, and health burden of the hemoglobinopathies,” Cold Spring Harbor Perspectives in Medicine, vol. 2, no. 9, Article ID a011692, 2012. View at Publisher · View at Google Scholar
  2. R. C. Hardison, D. H. K. Chui, C. R. Riemer et al., “Access to a syllabus of human hemoglobin variants (1996) via the world wide web,” Hemoglobin, vol. 22, no. 2, pp. 113–127, 1998. View at Google Scholar · View at Scopus
  3. N. F. Olivieri, “The β-thalassemias,” The New England Journal of Medicine, vol. 341, no. 2, pp. 9–109, 1999. View at Google Scholar
  4. G. La Nasa, F. Argiolu, C. Giardini et al., “Unrelated bone marrow transplantation for β-thalassemia patients: the experience of the Italian bone marrow transplant group,” Annals of the New York Academy of Sciences, vol. 1054, pp. 186–195, 2005. View at Publisher · View at Google Scholar · View at Scopus
  5. A. Kuliev, S. Rechitsky, O. Verlinsky et al., “Preimplantation diagnosis and HLA typing for haemoglobin disorders,” Reproductive BioMedicine Online, vol. 11, no. 3, pp. 362–370, 2005. View at Google Scholar · View at Scopus
  6. J. Reichenbach, H. D. van Velde, M. de Rycke et al., “First successful bone marrow transplantation for X-linked chronic granulomatous disease by using preimplantation female gender typing and HLA matching,” Pediatrics, vol. 122, no. 3, pp. e778–e782, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. H. van de Velde, M. de Rycke, C. de Man et al., “The experience of two European preimplantation genetic diagnosis centres on human leukocyte antigen typing,” Human Reproduction, vol. 24, no. 3, pp. 732–740, 2009. View at Publisher · View at Google Scholar · View at Scopus
  8. A. M. Hellani, S. M. Akoum, E. S. Fadel, H. M. Yousef, and K. K. Abu-Amero, “Successful pregnancies after combined human leukocyte antigen direct genotyping and preimplantation genetic diagnosis utilizing multiple displacement amplification,” Saudi Medical Journal, vol. 33, pp. 1059–1064, 2012. View at Google Scholar
  9. F. Lamazou, J. Steffann, N. Frydman et al., “Preimplantation diagnosis with HLA typing: birth of the first double hope child in France,” Journal de Gynécologie Obstétrique et Biologie de la Reproduction, vol. 40, no. 7, pp. 682–686, 2011. View at Publisher · View at Google Scholar
  10. T. El-Toukhy, H. Bickerstaff, and S. Meller, “Preimplantation genetic diagnosis for haematologic conditions,” Current Opinion in Pediatrics, vol. 22, no. 1, pp. 28–34, 2010. View at Publisher · View at Google Scholar · View at Scopus
  11. R. A. Smith, P. J. Ho, J. B. Clegg, J. R. Kidd, and S. L. Thein, “Recombination breakpoints in the human β-globin gene cluster,” Blood, vol. 92, no. 11, pp. 4415–4421, 1998. View at Google Scholar · View at Scopus
  12. G. L. Harton, M. de Rycke, F. Fiorentino et al., “ESHRE PGD consortium best practice guidelines for amplification-based PGD,” Human Reproduction, vol. 26, no. 1, pp. 33–40, 2011. View at Publisher · View at Google Scholar · View at Scopus
  13. A. Peciña, M. D. Lozano-Arana, J. C. García-Lozano, S. Borrego, and G. Antiñolo, “One-step multiplex polymerase chain reaction for preimplantation genetic diagnosis of Huntington disease,” Fertility and Sterility, vol. 93, no. 7, pp. 2411–2412, 2010. View at Google Scholar · View at Scopus
  14. R. Carrillo-Vadillo, J. C. García-Lozano, M. D. Lozano-Arana, J. L. M. Rivera, P. Sánchez Martín, and G. Antiñolo, “Two sets of monozygotic twins after intracytoplasmic sperm injection and transfer of two embryos on day 2,” Fertility and Sterility, vol. 88, no. 6, pp. 1676.e3–1676.e5, 2007. View at Publisher · View at Google Scholar · View at Scopus
  15. I. Liebaers, K. Sermon, C. Staessen et al., “Clinical experience with preimplantation genetic diagnosis and intracytoplasmic sperm injection,” Human Reproduction, vol. 13, supplement 1, pp. 186–195, 1998. View at Google Scholar · View at Scopus
  16. A. R. Thornhill, C. E. deDie-Smulders, J. P. Geraedts et al., “ESHRE PGD Consortium ‘best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)’,” Human Reproduction, vol. 20, no. 1, pp. 35–48, 2005. View at Publisher · View at Google Scholar · View at Scopus
  17. L. Malfroy, M. P. Roth, M. Carrington et al., “Heterogeneity in rates of recombination in the 6-Mb region telomeric to the human major histocompatibility complex,” Genomics, vol. 43, no. 2, pp. 226–231, 1997. View at Publisher · View at Google Scholar · View at Scopus
  18. M. Martin, D. Mann, and M. Carrington, “Recombination rates across the HLA complex: use of microsatellites as a rapid screen for recombinant chromosomes,” Human Molecular Genetics, vol. 4, no. 3, pp. 423–428, 1995. View at Google Scholar · View at Scopus
  19. H. van de Velde, I. Georgiou, M. de Rycke et al., “Novel universal approach for preimplantation genetic diagnosis of β-thalassaemia in combination with HLA matching of embryos,” Human Reproduction, vol. 19, no. 3, pp. 700–708, 2004. View at Publisher · View at Google Scholar · View at Scopus