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Results:
1-7
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Results: 7
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:
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:
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
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:
1-7
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