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Results: 1-9 |
Results: 9
Human sphingosine-1-phosphate lyase: cDNA cloning, functional expression studies and mapping to chromosome 10q22
Authors: Van Veldhoven, PP Gijsbers, S Mannaerts, GP Vermeesch, JR Brys, V
Citation: Pp. Van Veldhoven et al., Human sphingosine-1-phosphate lyase: cDNA cloning, functional expression studies and mapping to chromosome 10q22, BBA-MOL C B, 1487(2-3), 2000, pp. 128-134
Characterization of centromere alterations in liposarcomas
Authors: Sirvent, N Forus, A Lescaut, W Burel, F Benzaken, S Chazal, M Bourgeon, A Vermeesch, JR Myklebost, O Turc-Carel, C Ayraud, N Coindre, JM Pedeutour, F
Citation: N. Sirvent et al., Characterization of centromere alterations in liposarcomas, GENE CHROM, 29(2), 2000, pp. 117-129
Microdissection and FISH investigations in acute myeloid leukemia: A step forward to full identification of complex karyotypic changes
Authors: Falzetti, D Vermeesch, JR Matteucci, C Ciolli, S Martelli, MF Marynen, P Mecucci, C
Citation: D. Falzetti et al., Microdissection and FISH investigations in acute myeloid leukemia: A step forward to full identification of complex karyotypic changes, CANC GENET, 118(1), 2000, pp. 28-34
Cryptic translocation t(5;18) in familial mental retardation
Authors: Vogels, A Devriendt, K Vermeesch, JR Van Dael, R Marynen, P Dewaele, P Hageman, J Holvoet, M Fryns, JP
Citation: A. Vogels et al., Cryptic translocation t(5;18) in familial mental retardation, ANN GENET, 43(3-4), 2000, pp. 117-123
Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male
Authors: Vermeesch, JR Duhamel, H Petit, P Falzetti, D Fryns, JP Marynen, P
Citation: Jr. Vermeesch et al., Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male, HUM GENET, 105(6), 1999, pp. 611-618
Conserved DNA sequences adjacent to chromosome fragmentation and telomere addition sites in Euplotes crassus (vol 26, pg 4230, 1998)
Authors: Klobutcher, LA Gygax, SE Podoloff, JD Vermeesch, JR Price, CM Tebeau, CM Jahn, CL
Citation: La. Klobutcher et al., Conserved DNA sequences adjacent to chromosome fragmentation and telomere addition sites in Euplotes crassus (vol 26, pg 4230, 1998), NUCL ACID R, 27(4), 1999, pp. NIL_8-NIL_8
Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study
Authors: Falzetti, D Vermeesch, JR Hood, TL Nacheva, EP Matteucci, C Martelli, MF Van den Berghe, H Marynen, P Mecucci, C
Citation: D. Falzetti et al., Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study, LEUK RES, 23(4), 1999, pp. 407-413
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1
Authors: Devriendt, K Matthijs, G Van Dael, R Gewillig, M Eyskens, B Hjalgrim, H Dolmer, B McGaughran, J Brondum-Nielsen, K Marynen, P Fryns, JP Vermeesch, JR
Citation: K. Devriendt et al., Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1, AM J HU GEN, 64(4), 1999, pp. 1119-1126
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion
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
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