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Results: 1-25/32
Authors:
Stouffs, K
Lissens, W
Van Landuyt, L
Tournaye, H
Van Steirteghem, A
Liebaers, I
Citation: K. Stouffs et al., Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4), MOL HUM REP, 7(7), 2001, pp. 603-610
Authors:
Van Landuyt, L
Lissens, W
Stouffs, K
Tournaye, H
Van Steirteghem, A
Liebaers, I
Citation: L. Van Landuyt et al., The role of USP9Y and DBY in infertile patients with severely impaired spermatogenesis, MOL HUM REP, 7(7), 2001, pp. 691-692
Authors:
De Baere, E
Dixon, MJ
Small, KW
Jabs, EW
Leroy, BP
Devriendt, K
Gillerot, Y
Mortier, G
Meire, F
Van Maldergem, L
Courtens, W
Hjalgrim, H
Huang, S
Liebaers, I
Van Regemorter, N
Touraine, P
Praphanphoj, V
Verloes, A
Udar, N
Yellore, V
Chalukya, M
Yelchits, S
De Paepe, A
Kuttenn, F
Fellous, M
Veitia, R
Messiaen, L
Citation: E. De Baere et al., Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation, HUM MOL GEN, 10(15), 2001, pp. 1591-1600
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:
Collins, J
Evers, H
Golombok, S
Hannaford, P
Jacobs, HS
La Vecchia, C
Macunovich, DJ
Crosignani, PG
Devroey, P
Diedrich, K
Farley, T
Gianaroli, L
Liebaers, I
Persson, J
Quartarolo, JP
Ragni, G
Tarlatzis, B
Van Steirteghem, A
Diczfalusy, E
Rubin, BL
Citation: J. Collins et al., Social determinants of human reproduction, HUM REPR, 16(7), 2001, pp. 1518-1526
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:
Manning, M
Lissens, W
Liebaers, I
Van Steirteghem, A
Weidner, W
Citation: M. Manning et al., Imprinting analysis in spermatozoa prepared for intracytoplasmic sperm injection (ICSI), INT J ANDR, 24(2), 2001, pp. 87-94
Authors:
Manning, M
Lissens, W
Weidner, W
Liebaers, I
Citation: M. Manning et al., DNA methylation analysis in immature testicular sperm cells at different developmental stages, UROL INTERN, 67(2), 2001, pp. 151-155
Authors:
Van Landuyt, L
Lissens, W
Stouffs, K
Tournaye, H
Liebaers, I
Van Steirteghem, A
Citation: L. Van Landuyt et al., Validation of a simple Yq deletion screening programme in an ICSI candidate population, MOL HUM REP, 6(4), 2000, pp. 291-297
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:
Manning, M
Lissens, W
Bonduelle, M
Camus, M
De Rijcke, M
Liebaers, I
Van Steirteghem, A
Citation: M. Manning et al., Study of DNA-methylation patterns at chromosome 15q11-q13 in children bornafter ICSI reveals no imprinting defects, MOL HUM REP, 6(11), 2000, pp. 1049-1053
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:
Lissens, W
De Meirleir, L
Seneca, S
Liebaers, I
Brown, GK
Brown, RM
Ito, M
Naito, E
Kuroda, Y
Kerr, DS
Wexler, ID
Patel, MS
Robinson, BH
Seyda, A
Citation: W. Lissens et al., Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency, HUM MUTAT, 15(3), 2000, pp. 209-219
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:
Baird, DT
Collins, J
Cooke, I
Cohen, J
Evers, JLH
Glasier, A
Nieschlag, E
Van Steirteghem, A
Vercellini, P
Mishell, DR
Devroey, P
Diczfalusy, E
Diedrich, K
Edwards, RG
Engels, S
Liebaers, I
Lindner, A
Ragni, G
Tarlatzis, BC
Crosignani, PG
Rubin, BL
Citation: Dt. Baird et al., Optimal use of infertility diagnostic tests and treatments, HUM REPR, 15(3), 2000, pp. 723-732
Authors:
Vegetti, W
Van Assche, E
Frias, A
Verheyen, G
Bianchi, MM
Bonduelle, M
Liebaers, I
Van Steirteghem, A
Citation: W. Vegetti et al., Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in-situ hybridization in infertile men, HUM REPR, 15(2), 2000, pp. 351-365
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:
Cardozo, AK
De Meirleir, L
Liebaers, I
Lissens, W
Citation: Ak. Cardozo et al., Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency, PEDIAT RES, 48(6), 2000, pp. 748-753
Authors:
De Catte, L
Liebaers, I
Foulon, W
Citation: L. De Catte et al., Outcome of twin gestations after first trimester chorionic villus sampling, OBSTET GYN, 96(5), 2000, pp. 714-720
Authors:
Van Assche, E
Straessen, C
Vegetti, W
Bonduelle, M
Vandervorst, M
Van Steirteghem, A
Liebaers, I
Citation: E. Van Assche et al., Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22), MOL HUM REP, 5(7), 1999, pp. 682-690
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:
Staessen, C
Van Assche, E
Joris, H
Bonduelle, M
Vandervorst, M
Liebaers, I
Van Steirteghem, A
Citation: C. Staessen et al., Clinical experience of sex determination by fluorescent in-situ hybridization for preimplantation genetic diagnosis, MOL HUM REP, 5(4), 1999, pp. 382-389
Authors:
Lissens, W
Mahmoud, KZ
El-Gindi, E
Abdel-Sattar, A
Seneca, S
Van Steirteghem, A
Liebaers, I
Citation: W. Lissens et al., Molecular analysis of the cystic fibrosis gene reveals a high frequency ofthe intron 8 splice variant 5T in Egyptian males with congenital bilateralabsence of the vas deferens, MOL HUM REP, 5(1), 1999, pp. 10-13