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Results:
1-21
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Results: 21
Authors:
Khoo, SK
Bradley, M
Wong, FK
Hedblad, MA
Nordenskjold, M
Teh, BT
Citation: Sk. Khoo et al., Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2, ONCOGENE, 20(37), 2001, pp. 5239-5242
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:
Grigelioniene, G
Schoumans, J
Neumeyer, L
Ivarsson, SA
Eklof, O
Enkvist, O
Tordai, P
Fosdal, I
Myhre, AG
Westphal, O
Nilsson, NO
Elfving, M
Ellis, I
Anderlid, BM
Fransson, I
Tapia-Paez, I
Nordenskjold, M
Hagenas, L
Dumanski, JP
Citation: G. Grigelioniene et al., Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity, HUM GENET, 109(5), 2001, pp. 551-558
Authors:
Soderhall, C
Bradley, M
Kockum, I
Wahlgren, CF
Luthman, H
Nordenskjold, M
Citation: C. Soderhall et al., Linkage and association to candidate regions in Swedish atopic dermatitis families, HUM GENET, 109(2), 2001, pp. 129-135
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:
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:
Ericson, KG
Fadeel, B
Nilsson-Ardnor, S
Soderhall, C
Samuelsson, A
Janka, G
Schneider, M
Gurgey, A
Yalman, N
Revesz, T
Egeler, RM
Jahnukainen, K
Storm-Mathiesen, I
Haraldsson, A
Poole, J
de Saint Basile, G
Nordenskjold, M
Henter, JI
Citation: Kg. Ericson et al., Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis, AM J HU GEN, 68(3), 2001, pp. 590-597
Authors:
Lindblom, A
Nordenskjold, M
Citation: A. Lindblom et M. Nordenskjold, The biology of inherited cancer, SEM CANC B, 10(4), 2000, pp. 251-254
Authors:
Wong, FK
Burgess, J
Nordenskjold, M
Larsson, C
Teh, BT
Citation: Fk. Wong et al., Multiple endocrine neoplasia type 1, SEM CANC B, 10(4), 2000, pp. 299-312
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:
Bjorck, EJ
Bui, TH
Wijmenga, C
Grandell, U
Nordenskjold, M
Citation: Ej. Bjorck et al., Early prenatal diagnosis of the ICF syndrome, PRENAT DIAG, 20(10), 2000, pp. 828-831
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:
Bradley, M
Kockum, I
Soderhall, C
van Hage-Hamsten, M
Luthman, H
Nordenskjold, M
Wahlgren, CF
Citation: M. Bradley et al., Characterization by phenotype of families with atopic dermatitis, ACT DER-VEN, 80(2), 2000, pp. 106-110
Authors:
Li, CD
Berx, G
Larsson, C
Auer, G
Aspenblad, U
Pan, Y
Sundelin, B
Ekman, P
Nordenskjold, M
van Roy, F
Bergerheim, USR
Citation: Cd. Li et al., Distinct deleted regions on chromosome segment 16q23-24 associated with metastases in prostate cancer, GENE CHROM, 24(3), 1999, pp. 175-182
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:
Lindblom, A
Nordenskjold, M
Citation: A. Lindblom et M. Nordenskjold, Hereditary cancer, ACTA ONCOL, 38(4), 1999, pp. 439-447
Authors:
Teh, BT
Larsson, C
Nordenskjold, M
Citation: Bt. Teh et al., Tumor suppressor genes (TSG), ANTICANC R, 19(6A), 1999, pp. 4715-4728
Authors:
Carlson, KM
Gruber, A
Liliemark, E
Larsson, R
Nordenskjold, M
Citation: Km. Carlson et al., Characterization of drug-resistant cell lines by comparative genomic hybridization, CANC GENET, 111(1), 1999, pp. 32-36
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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