1. 2009
  2. Generation of lung epithelial-like tissue from human embryonic stem cells

    Van Haute, L., De Block, G., Liebaers, I., Sermon, K. & De Rycke, M., 5 Nov 2009, In : Respir Res. 10, November, p. 105-105 1 p.

    Research output: Contribution to journalArticle

  3. Cumulative reproductive outcome after preimplantation genetic diagnosis: a report on 1498 couples

    Verpoest, W., Haentjens, P., De Rycke, M., Staessen, C., Sermon, K., Bonduelle, M-L., Devroey, P. & Liebaers, I., Nov 2009, In : Hum Reprod. 24, November, p. 2951-2959 9 p.

    Research output: Contribution to journalArticle

  4. Mutation analysis of the NEMO gene in patients with Incontinentia Pigmenti.

    Lissens, W., Bonduelle, M-L., Seneca, S., Van Dooren, S. & Liebaers, I., 1 Oct 2009, Abstract of the 59th meeting ASHG, Hawaii, US. 1 p.

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

  5. Molecular spectrum of androgen receptor gene alterations in Belgian patients.

    Van Dooren, S., Vijzelaar, M., Seneca, S., De Rycke, M., Liebaers, I. & Lissens, W., 23 May 2009, In : Eur J Hum Genet. 17, p. 312-312 1 p.

    Research output: Contribution to journalConference paper

  6. Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6.

    Seneca, S., Dermaut, B., Santens, P., Dom, L., Smets, K., Ceulemans, L., Smet, J., De Paepe, B., Tousseyn, S., Weckhuysen, S., Gewillig, M., Pals, P., Parizel, P., De Bleecker, J., Boon, P., De Meirleir, L., De Jonghe, P., Vancoster, R., Van Paesschen, W., Lissens, W. & 1 others, Liebaers, I., 23 May 2009, In : Eur J Hum Genet. 17, p. 354-354 1 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  7. The experience of two European preimplantation genetic diagnosis centres on human leukocyte antigen typing

    Van De Velde, H., De Rycke, M., De Man, C., De Hauwere, K., Fiorentino, F., Kahraman, S., Pennings, G., Verpoest, W., Devroey, P. & Liebaers, I., Mar 2009, In : Hum Reprod. 24, March, p. 732-740 8 p.

    Research output: Contribution to journalArticle

  8. Infantile neuroaxonal dystrophy: challenges for identification and new advances in prenatal diagnosis

    Lissens, W., Buysse, G., Misson, J., Lagae, L., Ceuterick-De Groote, C., Vancoster, R., Schmedding, E., Seneca, S., Van Dooren, S., Liebaers, I. & De Meirleir, L., 13 Feb 2009, Abstract book of the 9th Annual Meeting of the Belgian Society of Human Genetics. p. 73-73 1 p.

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

  9. Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy

    Seneca, S., Meulemans, A., De Paepe, B., De Bleecker, J., Smet, J., De Meirleir, L., Lissens, W., Vancoster, R. & Liebaers, I., 13 Feb 2009, Abstract book of the 9th Annual Meeting of the Belgian Society of Human Genetics. p. 81-81 1 p.

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

Previous 1...3 4 5 6 7 8 9 10 ...51 Next

ID: 41145