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Results:
1-12
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Results: 12
Authors:
Van Limbergen, H
Poppe, B
Michaux, L
Herens, C
Brown, J
Noens, L
Berneman, Z
De Bock, R
De Paepe, A
Speleman, F
Citation: H. Van Limbergen et al., Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH, GENE CHROM, 33(1), 2002, pp. 60-72
Authors:
Verloes, A
Gillerot, Y
Van Maldergem, L
Schoos, R
Herens, C
Jamar, M
Dideberg, V
Lesenfants, S
Koulischer, L
Citation: A. Verloes et al., Major decrease in the incidence of trisomy21 at birth in south Belgium: mass impact of triple test?, EUR J HUM G, 9(1), 2001, pp. 1-4
Authors:
Riegel, M
Baumer, A
Jamar, M
Delbecque, K
Herens, C
Verloes, A
Schinzel, A
Citation: M. Riegel et al., Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes, HUM GENET, 109(3), 2001, pp. 286-294
Authors:
Herens, C
Thiry, A
Dresse, MF
Born, J
Flagothier, C
Vanstraelen, G
Allington, N
Bex, V
Citation: C. Herens et al., Translocation (16;17)(q22;p13) is a recurrent anomaly of aneurysmal bone cysts, CANC GENET, 127(1), 2001, pp. 83-84
Authors:
Verloes, A
Jamar, M
Dideberg, V
Herens, C
Citation: A. Verloes et al., Episphalosomic syndrome: a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens, ANN GENET, 44(2), 2001, pp. 59-62
Authors:
Michaux, L
Wlodarska, I
Stul, M
Dierlamm, J
Mugneret, F
Herens, C
Beverloo, B
Verhest, A
Verellen-Dumoulin, C
Verhoef, G
Selleslag, M
Madoe, V
Lecomte, M
Deprijck, B
Ferrant, A
Delannoy, A
Marichal, S
Duhem, C
Dicato, M
Hagemeijer, A
Citation: L. Michaux et al., MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23, GENE CHROM, 29(1), 2000, pp. 40-47
Authors:
Tassin, F
Dewe, W
Schaaf, N
Herens, C
Ravoet, C
Albert, A
Beguin, Y
Paulus, JM
Citation: F. Tassin et al., A four-parameter index of marrow dysplasia has predictive value for survival in myelodysplastic syndromes, LEUK LYMPH, 36(5-6), 2000, pp. 485-496
Authors:
Scantamburlo, G
Lampertz, S
Croisiau, C
Jamar, M
Koulischer, L
Herens, C
Citation: G. Scantamburlo et al., Inv(12)(q15q24): A nonrandom change associated with myelodysplasia?, CANC GENET, 121(2), 2000, pp. 206-207
Authors:
Verloes, A
Lesenfants, S
Jamar, M
Dideberg, V
Herens, C
Citation: A. Verloes et al., GOMBO syndrome: Another "pseudorecessive" disorder due to a cryptic translocation, AM J MED G, 95(2), 2000, pp. 185-186
Authors:
Herens, C
Tassin, F
Lemaire, V
Beguin, Y
Collard, E
Lampertz, S
Croisiau, C
Lecomte, M
De Prijk, B
Longree, L
Koulischer, L
Citation: C. Herens et al., Deletion of the 5 '-ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia-positive chronic myeloid leukaemia patients, BR J HAEM, 110(1), 2000, pp. 214-216
Authors:
Herens, C
Hermanne, JP
Tassin, F
Fassotte, MF
Thiry, A
Jamar, M
Schaaf-Lafontaine, N
Fillet, G
Koulischer, L
Citation: C. Herens et al., Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosis, CANC GENET, 110(1), 1999, pp. 62-64
Authors:
Herens, C
Brasseur, E
Jamar, M
Vierset, L
Schoenen, I
Koulischer, L
Citation: C. Herens et al., Loss of the Y chromosome in bone marrow cells: results on 1907 consecutivecases of leukaemia and preleukaemia, CLIN LAB H, 21(1), 1999, pp. 17-20
Risultati:
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