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Results:
1-23
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Results: 23
Authors:
Kalantari, M
Blennow, E
Hagmar, B
Johansson, B
Citation: M. Kalantari et al., Physical state of HPV16 and chromosomal mapping of the integrated form in cervical carcinomas, DIAGN MOL P, 10(1), 2001, pp. 46-54
Authors:
Bruder, CEG
Hirvela, C
Tapia-Paez, I
Fransson, I
Segraves, R
Hamilton, G
Zhang, XX
Evans, DG
Wallace, AJ
Baser, ME
Zucman-Rossi, J
Hergersberg, M
Boltshauser, E
Papi, L
Rouleau, GA
Poptodorov, G
Jordanova, A
Rask-Andersen, H
Kluwe, L
Mautner, V
Sainio, M
Hung, G
Mathiesen, T
Moller, C
Pulst, SM
Harder, H
Heiberg, A
Honda, M
Miimura, M
Sahlen, S
Blennow, E
Albertson, DG
Pinkel, D
Dumanski, JP
Citation: Ceg. Bruder et al., High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH, HUM MOL GEN, 10(3), 2001, pp. 271-282
Authors:
Nordgren, A
Farnebo, F
Johansson, B
Holmgren, G
Forestier, E
Larsson, C
Soderhall, S
Nordenskjold, M
Blennow, E
Citation: A. Nordgren et al., Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping, EUR J HAEMA, 66(5), 2001, pp. 297-304
Authors:
Lindvall, C
Nordenskjold, M
Porwit, A
Bjorkholm, M
Blennow, E
Citation: C. Lindvall et al., Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements, HAEMATOLOG, 86(11), 2001, pp. 1158-1164
Authors:
Tapia-Paez, I
Kost-Alimova, M
Hu, P
Roe, BA
Blennow, E
Fedorova, L
Imreh, S
Dumanski, JP
Citation: I. Tapia-paez et al., The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers, HUM GENET, 109(2), 2001, pp. 167-177
Authors:
Fridstrom, M
Ahrlund-Richter, L
Iwarsson, E
Malmgren, H
Inzunza, J
Rosenlund, B
Sjoblom, P
Nordenskjold, M
Blennow, E
Hovatta, O
Citation: M. Fridstrom et al., Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities, PRENAT DIAG, 21(9), 2001, pp. 781-787
Authors:
Anderlid, BM
Sahlen, S
Schoumans, J
Holmberg, E
Ahsgren, I
Mortier, G
Speleman, F
Blennow, E
Citation: Bm. Anderlid et al., Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy, AM J MED G, 99(3), 2001, pp. 223-233
Authors:
Nordgren, A
Schoumans, J
Soderhall, S
Nordenskjold, M
Blennow, E
Citation: A. Nordgren et al., Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotype, BR J HAEM, 114(4), 2001, pp. 786-793
Authors:
Lee, C
Gisselsson, D
Jin, C
Nordgren, A
Ferguson, DO
Blennow, E
Fletcher, JA
Morton, CC
Citation: C. Lee et al., Limitations of chromosome classification by multicolor karyotyping, AM J HU GEN, 68(4), 2001, pp. 1043-1047
Authors:
Zheng, C
Pisa, P
Stromberg, O
Blennow, E
Hansson, M
Citation: C. Zheng et al., Generation of dendritic cells from peripheral blood of patients at different stages of chronic myeloid leukemia, MED ONCOL, 17(4), 2000, pp. 270-278
Authors:
Nordgren, A
Sorensen, AG
Tinggaard-Pedersen, N
Blennow, E
Larsson, C
Lagercrantz, S
Citation: A. Nordgren et al., New chromosomal breakpoints in non-Hodgkin's lymphomas revealed by spectral karyotyping and G-banding, INT J MOL M, 5(5), 2000, pp. 485-492
Authors:
Bergman, A
Blennow, E
Citation: A. Bergman et E. Blennow, Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorgesyndrome, EUR J HUM G, 8(10), 2000, pp. 801-804
Authors:
Tapia-Paez, I
O'Brien, KP
Kost-Alimova, M
Sahlen, S
Kedra, D
Bruder, CEG
Andersson, B
Roe, BA
Hu, P
Imreh, S
Blennow, E
Dumanski, JP
Citation: I. Tapia-paez et al., Fine mapping of the constitutional translocation t(11;22)(q23;q11), HUM GENET, 106(5), 2000, pp. 506-516
Authors:
De Boer, K
Hussey, N
Wilton, L
Sermon, K
Hindkjaer, J
Frydman, N
Viville, S
Kanavakis, E
Kontogianni, E
Manor, D
Ciotti, MP
Magli, C
Coonen, E
Kang, IS
Veiga, A
Santalo, J
Blennow, E
Braude, P
Harper, J
Lavery, S
Miller, K
Agan, N
Drury, K
Gitlin, S
Krey, L
Munne, S
Citation: K. De Boer et al., ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: data collection II (May 2000), HUM REPR, 15(12), 2000, pp. 2673-2683
Authors:
Iwarsson, E
Malmgren, H
Inzunza, J
Ahrlund-Richter, L
Sjoblom, P
Rosenlund, B
Fridstrom, M
Hovatta, O
Nordenskjold, M
Blennow, E
Citation: E. Iwarsson et al., Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers, PRENAT DIAG, 20(13), 2000, pp. 1038-1047
Authors:
Tsezou, A
Kitsiou, S
Galla, A
Petersen, MB
Karadima, G
Syrrou, M
Sahlen, S
Blennow, E
Citation: A. Tsezou et al., Molecular cytogenetic characterization and origin of two de novo duplication 9p cases, AM J MED G, 91(2), 2000, pp. 102-106
Authors:
Zhang, AJ
Zheng, CY
Lindvall, C
Hou, M
Ekedahl, J
Lewensohn, R
Yan, ZQ
Yang, XY
Henriksson, M
Blennow, E
Nordenskjold, M
Zetterberg, A
Bjorkholm, M
Gruber, A
Xu, DW
Citation: Aj. Zhang et al., Frequent amplification of the Telomerase Reverse Transcriptase gene in human tumors, CANCER RES, 60(22), 2000, pp. 6230-6235
Authors:
Bruder, CEG
Ichimura, K
Blennow, E
Ikeuchi, T
Yamaguchi, T
Yuasa, Y
Collins, VP
Dumanski, JP
Citation: Ceg. Bruder et al., Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: Possible localization of a neurofibromatosis type 2 modifier gene?, GENE CHROM, 25(2), 1999, pp. 184-190
Authors:
Iwarsson, E
Lundqvist, M
Inzunza, J
Ahrlund-Richter, L
Sjoblom, P
Lundkvist, O
Simberg, N
Nordenskjold, M
Blennow, E
Citation: E. Iwarsson et al., A high degree of aneuploidy in frozen-thawed human preimplantation embryos, HUM GENET, 104(5), 1999, pp. 376-382
Authors:
Bjorck, EJ
Anderlid, BM
Blennow, E
Citation: Ej. Bjorck et al., Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q), AM J MED G, 87(1), 1999, pp. 49-52
Authors:
Blennow, E
Sahlen, S
Citation: E. Blennow et S. Sahlen, Rescue from the effects of trisomy 13q32 -> qter owing to skewed X inactivation in a der(X)t(X;13) (p21;q32) carrier, J MED GENET, 36(9), 1999, pp. 718-719
Authors:
Vorechovsky, I
Blennow, E
Nordenskjold, M
Webster, ADB
Hammarstrom, L
Citation: I. Vorechovsky et al., A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: Evidence from meiotic mapping of 83 multiple-case families, J IMMUNOL, 163(4), 1999, pp. 2236-2242
Authors:
Inzunza, J
Iwarsson, E
Fridstrom, M
Rosenlund, B
Sjoblom, P
Hillensjo, T
Blennow, E
Jones, B
Nordenskjold, M
Ahrlund-Richter, L
Citation: J. Inzunza et al., Application of single-needle blastomere biopsy in human preimplantation genetic diagnosis, PRENAT DIAG, 18(13), 1998, pp. 1381-1388
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