1. 1999
  2. Preimplantation diagnosis for fragile X-syndrome based on the detection of the non-expanded paternal and maternal CGG

    Sermon, K., Seneca, S., Vanderfaeillie, A., Lissens, W., Joris, H., Vandervorst, M., Van Steirteghem, A. & Liebaers, I., Dec 1999, In : Prenat Diagn. 19, December, p. 1223-1230 8 p.

    Research output: Contribution to journalArticle

  3. Fluorescent PCR and automated fragment analysis in preimplantaion gentic diagnosis for 21-hydroxylase deficiency in congenital adrenal hyperplasia.

    Van De Velde, H., Sermon, K., De Vos, A., Lissens, W., Joris, H., Vandervorst, M., Van Steirteghem, A. & Liebaers, I., Jul 1999, In : Molecular Human Reproduction. 5, July, p. 691-696 6 p.

    Research output: Contribution to journalArticle

  4. Preimplantation genetic diagnosis and sperm analysis by fluorescence insitu hybridisation for the most common reciprocal translocation t(11;22)

    Van Assche, E., Staessen, C., Vegetti, W., Bonduelle, M-L., Vandervorst, M., Van Steirteghem, A. & Liebaers, I., Jul 1999, In : Molecular Human Reproduction. 5, July, p. 682-690 9 p.

    Research output: Contribution to journalArticle

  5. Clinical experience of sex determination by fluorescent in-situ hybridization for preimplantation genetic diagnosis.

    Staessen, C., Van Assche, E., Joris, H., Bonduelle, M-L., Vandervorst, M., Liebaers, I. & Van Steirteghem, A., Apr 1999, In : Molecular Human Reproduction. 5, April, p. 382-390 9 p.

    Research output: Contribution to journalArticle

  6. Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferens

    Lissens, W., Mahmoud, K. Z., El-Gindi, E., Abdel-Sattar, A., Seneca, S., Van Steirteghem, A. & Liebaers, I., Jan 1999, In : Molecular Human Reproduction. 5, 1, p. 10-13 4 p.

    Research output: Contribution to journalArticle

  7. Preimplantation genetic diagnosis of Marfan syndrome with the use of fluorescent polymerase chain reaction and the automated laser fluorescent DNA sequencer.

    Sermon, K., Lissens, W., Messiaen, L., Bonduelle, M-L., Vandervorst, M., Van Steirteghem, A. & Liebaers, I., Jan 1999, In : Fertil Steril. 71, January, p. 163-166 4 p.

    Research output: Contribution to journalArticle

  8. BRCA 1/2 gene mutation testing-based cancer prevention and the moral concerns of different types of patients

    Goelen, G., Rigo, A., Bonduelle, M-L. & De Greve, J., 1999, Unknown Journal.

    Research output: Contribution to specialist/vulgarizing publicationArticleSpecialist

  9. Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene

    Lissens, W., Vreken, P., Barth, P. G., Wijburg, F. A., Ruitenbeek, W., Wanders, R. J., Seneca, S., Liebaers, I. & De Meirleir, L., 1999, In : European Journal of Pediatrics. 158, 10, p. 853-857 5 p.

    Research output: Contribution to journalArticle

  10. Cerebral palsy and pyruvate dehydrogenase deficiency: identification od two new mutations in the Ela gene.

    Lissens, W., Vreken, P., Barth, P. G., Wijburg, F. A., Ruitenbeek, W., Wanders, R. J. A., Seneca, S., Liebaers, I. & De Meirleir, L., 1999, In : Unknown Journal.

    Research output: Contribution to journalArticle

  11. Clinical experience with PID and ICSI in 'Genetics in Human reproduction'

    Van Assche, E., Van Steirteghem, A., Liebaers, I., Bonduelle, M-L., Devroey, P., Graumann, S. (ed.), Hildt, E. (ed.), Joris, C., Lissens, W., Nagy, P., Sermon, K., Staessen, C. & Vandervorst, M., 1999, In book Genetics in human reproduction, E. Hildt, S. Graumann (eds), p3-15, 1999..

    Research output: Chapter in Book/Report/Conference proceedingChapter

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