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Results:
1-14
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Results: 14
Authors:
Georgiou, I
Sermon, K
Lissens, W
De Vos, A
Platteau, P
Lolis, D
Van Steirteghem, A
Liebaers, I
Citation: I. Georgiou et al., Preimplantation genetic diagnosis for spinal and bulbar muscular atrophy (SBMA), HUM GENET, 108(6), 2001, pp. 494-498
Authors:
Sermon, K
Seneca, S
De Rycke, M
Goossens, V
Van de Velde, H
De Vos, A
Platteau, P
Lissens, W
Van Steirteghem, A
Liebaers, I
Citation: K. Sermon et al., PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome, MOL C ENDOC, 183, 2001, pp. S77-S85
Authors:
De Rycke, M
Van de Velde, H
Sermon, K
Lissens, W
De Vos, A
Vandervorst, M
Vanderfaeillie, A
Van Steirteghem, A
Liebaers, I
Citation: M. De Rycke et al., Preimplantation genetic diagnosis for sickle-cell anemia and for beta-thalassemia, PRENAT DIAG, 21(3), 2001, pp. 214-222
Authors:
Sermon, K
Henderix, P
Lissens, W
De Vos, A
Vandervorst, M
Vanderfaeillie, A
Vamos, E
Van Steirteghem, A
Liebaers, I
Citation: K. Sermon et al., Preimplantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, MOL HUM REP, 6(12), 2000, pp. 1165-1168
Authors:
Vandervorst, M
Staessen, C
Sermon, K
De Vos, A
Van de Velde, H
Van Assche, E
Bonduelle, M
Vanderfaellie, A
Lissens, W
Tournaye, H
Devroey, P
Van Steirteghem, A
Liebaers, I
Citation: M. Vandervorst et al., The Brussels' experience of more than 5 years of clinical preimplantation genetic diagnosis, HUM REP UPD, 6(4), 2000, pp. 364-373
Authors:
De Vos, A
Sermon, K
Van de Velde, H
Joris, H
Vandervorst, M
Lissens, W
De Paepe, A
Liebaers, I
Van Steirteghem, A
Citation: A. De Vos et al., Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV, HUM GENET, 106(6), 2000, pp. 605-613
Authors:
De Boer, K
Hussey, N
Wilton, L
Sermon, K
Hindkjaer, J
Frydman, N
Viville, S
Kanavakis, E
Kontogianni, E
Manor, D
Ciotti, MP
Magli, C
Coonen, E
Kang, IS
Veiga, A
Santalo, J
Blennow, E
Braude, P
Harper, J
Lavery, S
Miller, K
Agan, N
Drury, K
Gitlin, S
Krey, L
Munne, S
Citation: K. De Boer et al., ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: data collection II (May 2000), HUM REPR, 15(12), 2000, pp. 2673-2683
Authors:
Goossens, V
Sermon, K
Lissens, W
Vandervorst, M
Vanderfaeillie, A
De Rijcke, M
De Vos, A
Henderix, P
Van de Velde, H
Van Steirteghem, A
Liebaers, I
Citation: V. Goossens et al., Clinical application of preimplantation genetic diagnosis for cystic fibrosis, PRENAT DIAG, 20(7), 2000, pp. 571-581
Authors:
Van de Velde, H
De Vos, A
Sermon, K
Staessen, C
De Rycke, M
Van Assche, E
Lissens, W
Vandervorst, M
Van Ranst, H
Liebaers, I
Van Steirteghem, A
Citation: H. Van De Velde et al., Embryo implantation after biopsy of one or two cells from cleavage-stage embryos with a view to preimplantation genetic diagnosis, PRENAT DIAG, 20(13), 2000, pp. 1030-1037
Authors:
Van de Velde, H
Sermon, K
De Vos, A
Lissens, W
Joris, H
Vandervorst, M
Van Steirteghem, A
Liebaers, I
Citation: H. Van De Velde et al., Fluorescent PCR and automated fragment analysis in preimplantation geneticdiagnosis for 21-hydroxylase deficiency in congenital adrenal hyperplasia, MOL HUM REP, 5(7), 1999, pp. 691-696
Authors:
Geraedts, J
Handyside, A
Harper, J
Liebaers, I
Sermon, K
Staessen, C
Thornhill, A
Vanderfaeillie, A
Viville, S
Citation: J. Geraedts et al., ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: preliminary assessment of data from January 1997 to September 1998, HUM REPR, 14(12), 1999, pp. 3138-3148
Authors:
Sermon, K
Seneca, S
Vanderfaeillie, A
Lissens, W
Joris, H
Vandervorst, M
Van Steirteghem, A
Liebaers, I
Citation: K. Sermon et al., Preimplantation diagnosis for fragile X syndrome based on the detection ofthe non-expanded paternal and maternal CGG, PRENAT DIAG, 19(13), 1999, pp. 1223-1230
Authors:
Sermon, K
Lissens, W
Messiaen, L
Bonduelle, M
Vandervorst, M
Van Steirteghem, A
Liebaers, I
Citation: K. Sermon et al., Preimplantation genetic diagnosis of Marfan syndrome with the use of fluorescent polymerase chain reaction and the Automated Laser Fluorescence DNA Sequencer, FERT STERIL, 71(1), 1999, pp. 163-166
Authors:
Sermon, K
Goossens, V
Seneca, S
Lissens, W
De Vos, A
Vandervorst, M
Van Steirteghem, A
Liebaers, I
Citation: K. Sermon et al., Preimplantation diagnosis for Huntington's disease (HD): Clinical application and analysis of the HD expansion in affected embryos, PRENAT DIAG, 18(13), 1998, pp. 1427-1436
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