1. 2012
  2. Facilitating the Fragile X post- and prenatal genetic diagnostic testing workflow through the Abbott FraXa TP-PCR and sizing PCR.

    Van Dooren, S., Seneca, S., Endels, K., Keymolen, K., De Rademaeker, M., Van Berkel, K., Lissens, W. & Bonduelle, M-L., 2 Mar 2012, Abstract book of the 12th Annual Meeting of the Belgian Society of Human Genetics. p. 92-92 1 p.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract (Book)Research

  3. Identification of two de novo mutations responsible for type I antithrombin deficiency.

    Orlando, C., Lissens, W., Hasaerts, D. & Jochmans, K., Jan 2012, In : Thromb Haemost. 107, 2012, p. 187-189 3 p.

    Research output: Contribution to journalArticle

  4. Array comparative genomic hybridization in male infertility.

    Stouffs, K., Vandermaelen, D., Massart, A., Menten, B., Vergult, S., Tournaye, H. & Lissens, W., 2012, In : Hum Reprod. 27, March, p. 921-929 9 p.

    Research output: Contribution to journalArticle

  5. Genetic causes of spermatogenic failure

    Massart, A., Lissens, W., Tournaye, H. & Stouffs, K., 2012, In : Asian Journal of Andrology. 14, p. 40-48 9 p.

    Research output: Contribution to journalArticle

  6. 2011
  7. S-057 Brugada Sendromunda sodyum kanalı beta-alt birimlerinin genetik analizleri

    Komurcu-Bayrak, E., Endels, K., Lissens, W., Seneca, S., Bayrak, F., Sarkozy, A., Brugada, P., Bonduelle, M-L. & Van Dooren, S., 27 Oct 2011, XXVII. Ullusal Kardiyologji Kongresi : Supplementum. Turkey: Archives of the Turkish Society of Cardiology

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract (Book)Research

  8. Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutation

    Fiumara, A., R., B., Arena, A., M., F., Lissens, W., L., P. & Sorge, G., 10 Oct 2011, In : Clin Genet. 80, p. 452-458 7 p.

    Research output: Contribution to journalArticle

  9. Analysis of the giant axonal neuropathy fibroblasts proteome.

    Van Coster, R., Mussche, S., De Paepe, B., Smet, J., Lissens, W., Milic Rasic, V. & Devreese, B., Aug 2011, In : Journal of Inherited Metabolic Disease. 34, s3, p. s239 1 p., P-473.

    Research output: Contribution to journalMeeting abstract (Journal)

  10. ATP synthase deficiency: diagnostic strategies for not such an uncommon cause of OXPHOS dysfunction.

    Van Coster, R., Smet, J., De Paepe, B., Seneca, S., De Meirleir, L., Régal, L., Evangeliou, A. & Lissens, W., Aug 2011, In : Journal of Inherited Metabolic Disease. 34, p. 157-157 1 p.

    Research output: Contribution to journalConference paper

  11. Fluorescent visualization of the mitochondrial membrane potential gradient identifies oxidative phosphorylation defects in fibroblasts.

    Van Coster, R., De Paepe, B., Smet, J., Seneca, S., Lissens, W., De Meirleir, L. & Rodenburg, R., Aug 2011, In : Journal of Inherited Metabolic Disease. 34, p. 159-159 1 p.

    Research output: Contribution to journalConference paper

  12. A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperature

    Bissay, V., Keymolen, K., Lissens, W., Schmedding, E. & De Keyser, J., 14 Jul 2011, In : J Neurol Sci. 308, p. 162-164 3 p.

    Research output: Contribution to journalArticle

Previous 12 3 4 5 6 7 8 9 ...39 Next

ID: 48399