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Results:
1-19
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Results: 19
Authors:
Delvaux, I
Van Tongerloo, A
Messiaen, L
Van Loon, C
De Bie, S
Mortier, G
De Paepe, A
Citation: I. Delvaux et al., Carrier screening for cystic fibrosis in a prenatal setting, GENET TEST, 5(2), 2001, pp. 117-125
Authors:
Gross, C
De Baere, E
Lo, A
Chang, WH
Messiaen, L
Citation: C. Gross et al., Cloning and characterization of human WDR10, a novel gene located at 3q21 encoding a WD-repeat protein that is highly expressed in pituitary and testis, DNA CELL B, 20(1), 2001, pp. 41-52
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:
Van Vlierberghe, H
Delanghe, JR
De Bie, S
Praet, M
De Paepe, A
Messiaen, L
De Vos, M
Leroux-Roels, G
Citation: H. Van Vlierberghe et al., Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C, EUR J GASTR, 13(9), 2001, pp. 1077-1081
Authors:
Bassi, MT
Bergen, AAB
Bitoun, P
Charles, SJ
Clementi, M
Gosselin, R
Hurst, J
Lewis, RA
Lorenz, B
Meitinger, T
Messiaen, L
Ramesar, RS
Ballabio, A
Schiaffino, MV
Citation: Mt. Bassi et al., Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America, HUM GENET, 108(1), 2001, pp. 51-54
Authors:
De Baere, E
Fukushima, Y
Small, K
Udar, N
Van Camp, G
Verhoeven, K
Palotie, A
De Paepe, A
Messiaen, L
Citation: E. De Baere et al., Identification of BPESC1, a novel gene disrupted by a balanced chromosomaltranslocation, t(3;4)(q23;p15.2), in a patient with BPES, GENOMICS, 68(3), 2000, pp. 296-304
Authors:
De Keyser, F
Peene, I
Joos, R
Naeyaert, JM
Messiaen, L
Veys, EM
Citation: F. De Keyser et al., Occurrence of scleroderma in monozygotic twins, J RHEUMATOL, 27(9), 2000, pp. 2267-2269
Authors:
Lambert, J
Naeyaert, JM
De Paepe, A
Van Coster, R
Ferster, A
Song, M
Messiaen, L
Citation: J. Lambert et al., Arg-Cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndrome, J INVES DER, 114(4), 2000, pp. 731-733
Authors:
Mazoyer, S
Leary, J
Kirk, J
Fleischmann, E
Wagner, T
Claes, K
Messiaen, L
Foulkes, W
Desrochers, M
Simard, J
Phelan, CM
Kwan, E
Narod, SA
Vahteristo, P
Nevanlinna, H
Durando, X
Bignon, YJ
Peyrat, JP
Bonnardel, C
Sinilnikova, OM
Puget, N
Lenoir, GM
Mazoyer, S
Audoynaud, C
Goldgar, D
Maugard, C
Caux, V
Gad, S
Stoppa-Lyonnet, D
Nogues, C
Lidereau, R
Machavoine, C
Bressac-de Paillerets, B
Kuschel, B
Betz, B
Niederacher, D
Beckmann, MW
Hamann, U
Gayther, SA
Ponder, BAP
Robinson, M
Taylor, GR
Bishop, T
Catteau, A
Solomon, E
Cohen, B
Steel, M
Collins, N
Stratton, M
van der Looij, M
Olah, E
Miller, NJ
Barton, DE
Sverdlov, RS
Friedman, E
Radice, P
Montagna, M
Sensi, E
Caligo, M
van Eijk, R
Devilee, P
van der Luijt, R
Heimdal, K
Moller, P
Borg, A
Diez, O
Cortes, J
Domenech, M
Baiget, M
Osorio, A
Benitez, J
Borg, A
Maillet, P
Sappino, AP
Ozdag, H
Ozcelik, T
Ozturk, M
Rohlfs, EM
Boyd, J
McDermott, D
Offit, K
Unger, M
Nathanson, K
Weber, BL
Sellers, TA
Hampton, E
Couch, FJ
Neuhausen, S
Citation: S. Mazoyer et al., The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations, AM J HU GEN, 67(1), 2000, pp. 207-212
Prevalence of the Cys282Tyr and His63Asp mutation in flemish patients withhereditary hemochromatosis
Authors:
Van Vlierberghe, H
Messiaen, L
Hautekeete, M
De Paepe, A
Elewaut, A
Citation: H. Van Vlierberghe et al., Prevalence of the Cys282Tyr and His63Asp mutation in flemish patients withhereditary hemochromatosis, ACT GASTR B, 63(3), 2000, pp. 250-253
Authors:
De Baere, E
Van Roy, N
Speleman, F
Fukushima, Y
De Paepe, A
Messiaen, L
Citation: E. De Baere et al., Closing in an the BPES gene on 3q23: Mapping of a de nova reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta '-COP, distal to the breakpoint, GENOMICS, 57(1), 1999, pp. 70-78
Authors:
Foretova, L
Machackova, E
Valik, D
Messiaen, L
Citation: L. Foretova et al., The Czech Republic: Genetic counseling in high-risk breast/ovarian cancer families, DIS MARKER, 15(1-3), 1999, pp. 50-50
Authors:
Claes, K
Machackova, E
De Vos, M
Poppe, B
De Paepe, A
Messiaen, L
Citation: K. Claes et al., Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5+3A > G, DIS MARKER, 15(1-3), 1999, pp. 69-73
Authors:
De Vos, M
Poppe, B
Delvaux, I
Mortier, G
Claes, K
Messiaen, L
De Paepe, A
Citation: M. De Vos et al., Genetic counselling and testing for hereditary breast and ovarian cancer: The gent(le) approach, DIS MARKER, 15(1-3), 1999, pp. 191-195
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:
Courtens, W
Grossman, D
Van Roy, N
Messiaen, L
Vamos, E
Toppet, V
Haumont, D
Streydio, C
Jauch, A
Vermeesch, JR
Speleman, F
Citation: W. Courtens et al., Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion, HUM GENET, 103(4), 1998, pp. 497-505
Authors:
De Baere, E
Speleman, F
Van Roy, N
Mortier, K
De Paepe, A
Messiaen, L
Citation: E. De Baere et al., Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridization, CYTOG C GEN, 83(3-4), 1998, pp. 240-241
Authors:
De Baere, E
Speleman, F
Van Roy, N
De Paepe, A
Messiaen, L
Citation: E. De Baere et al., Assignment of the cellular retinol-binding protein 1 gene (RBP1) and of the coatomer beta ' subunit gene (COPB2) to human chromosome band 3q23 by in situ hybridization, CYTOG C GEN, 82(3-4), 1998, pp. 226-227
Authors:
De Baere, E
Speleman, F
Van Roy, N
De Paepe, A
Messiaen, L
Citation: E. De Baere et al., Assignment of SHOX2 (alias OG12X and SHOT) to human chromosome bands 3q25 -> q26.1 by in situ hybridization, CYTOG C GEN, 82(3-4), 1998, pp. 228-229
Risultati:
1-19
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