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THE MAJORITY OF METACHRONOUS CIN1 AND CIN3 LESIONS ARE CAUSED BY DIFFERENT HPV GENOTYPES, INDICATING THAT ACTUAL PROGRESSION OF CIN1 IS A RARE EVENT

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Chicago
Litjens, R., Koen Van de Vijver, A. H. N. Hopman, M. I. Ummelen, E. J. M. Speel, S. H. Sastrowijoto, T. Van Gorp, R. F. P. M. Kruitwagen, B. F. M. Slangen, and A. J. Kruse. 2013. “THE MAJORITY OF METACHRONOUS CIN1 AND CIN3 LESIONS ARE CAUSED BY DIFFERENT HPV GENOTYPES, INDICATING THAT ACTUAL PROGRESSION OF CIN1 IS A RARE EVENT.” International Journal of Gynecological Cancer 23 (8).
APA
Litjens, R., Van de Vijver, K., Hopman, A. H. N., Ummelen, M. I., Speel, E. J. M., Sastrowijoto, S. H., Van Gorp, T., et al. (2013). THE MAJORITY OF METACHRONOUS CIN1 AND CIN3 LESIONS ARE CAUSED BY DIFFERENT HPV GENOTYPES, INDICATING THAT ACTUAL PROGRESSION OF CIN1 IS A RARE EVENT. INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 23(8).
Vancouver
1.
Litjens R, Van de Vijver K, Hopman AHN, Ummelen MI, Speel EJM, Sastrowijoto SH, et al. THE MAJORITY OF METACHRONOUS CIN1 AND CIN3 LESIONS ARE CAUSED BY DIFFERENT HPV GENOTYPES, INDICATING THAT ACTUAL PROGRESSION OF CIN1 IS A RARE EVENT. INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER. 2013;23(8).
MLA
Litjens, R., Koen Van de Vijver, A. H. N. Hopman, et al. “THE MAJORITY OF METACHRONOUS CIN1 AND CIN3 LESIONS ARE CAUSED BY DIFFERENT HPV GENOTYPES, INDICATING THAT ACTUAL PROGRESSION OF CIN1 IS A RARE EVENT.” INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER 23.8 (2013): n. pag. Print.
@article{8589753,
  author       = {Litjens, R. and Van de Vijver, Koen and Hopman, A. H. N. and Ummelen, M. I. and Speel, E. J. M. and Sastrowijoto, S. H. and Van Gorp, T. and Kruitwagen, R. F. P. M. and Slangen, B. F. M. and Kruse, A. J.},
  issn         = {1048-891X},
  journal      = {INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER},
  number       = {8},
  title        = {THE MAJORITY OF METACHRONOUS CIN1 AND CIN3 LESIONS ARE CAUSED BY DIFFERENT HPV GENOTYPES, INDICATING THAT ACTUAL PROGRESSION OF CIN1 IS A RARE EVENT},
  volume       = {23},
  year         = {2013},
}

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