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Results: 1-10 |
Results: 10
Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families
Authors: Barkardottir, RB Sarantaus, L Arason, A Vehmanen, P Bendahl, PO Kainu, T Syrjakoski, K Krahe, R Huusko, P Pyrhonen, S Holli, K Kallioniemi, OP Egilsson, V Kere, J Nevanlinna, H
Citation: Rb. Barkardottir et al., Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families, EUR J HUM G, 9(10), 2001, pp. 773-779
The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
Authors: Lakhani, SR Gusterson, BA Jacquemier, J Sloane, JP Anderson, TJ van de Vijver, MJ Venter, D Freeman, A Antoniou, A McGuffog, L Smyth, E Steel, CM Haites, N Scott, RJ Goldgar, D Neuhausen, S Daly, PA Ormiston, W McManus, R Scherneck, S Ponder, BAJ Futreal, PA Peto, J Stoppa-Lyonnet, D Bignon, YJ Struewing, JP Bishop, DT Klijn, JGM Devilee, P Cornelisse, CJ Lasset, C Lenoir, G Barkardottir, RB Egilsson, V Hamann, U Chang-Claude, J Sobol, H Weber, B Easton, DF Stratton, MR
Citation: Sr. Lakhani et al., The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2, CLIN CANC R, 6(3), 2000, pp. 782-789
The effect of mismatch repair deficiency on tumourigenesis; microsatelliteinstability affecting genes containing short repeated sequences
Authors: Johannsdottir, JT Jonasson, JG Bergthorsson, JT Amundadottir, L Magnusson, J Egilsson, V Ingvarsson, S
Citation: Jt. Johannsdottir et al., The effect of mismatch repair deficiency on tumourigenesis; microsatelliteinstability affecting genes containing short repeated sequences, INT J ONCOL, 16(1), 2000, pp. 133-139
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
Authors: Kainu, T Juo, SHH Desper, R Schaffer, AA Gillanders, E Rozenblum, E Freas-Lutz, D Weaver, D Stephan, D Bailey-Wilson, J Kallioniemi, OP Tirkkonen, M Syrjakoski, K Kuukasjarvi, T Koivisto, P Karhu, R Holli, K Arason, A Johannesdottir, G Bergthorsson, JT Johannsdottir, H Egilsson, V Barkardottir, RB Johannsson, O Haraldsson, K Sandberg, T Holmberg, E Gronberg, H Olsson, H Borg, A Vehmanen, P Eerola, H Heikkila, P Pyrhonen, S Nevanlinna, H
Citation: T. Kainu et al., Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus, P NAS US, 97(17), 2000, pp. 9603-9608
Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer
Authors: Sigbjornsdottir, BI Ragnarsson, G Agnarsson, BA Chen, HP Barkardottir, RB Egilsson, V Ingvarsson, S
Citation: Bi. Sigbjornsdottir et al., Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer, J MED GENET, 37(5), 2000, pp. 342-347
Replication error in human breast cancer: Comparison with clinical variables and family history of cancer
Authors: Chen, HP Johannsdottir, JT Arason, A Olafsdottir, GH Eiriksdottir, G Egilsson, V Ingvarsson, S
Citation: Hp. Chen et al., Replication error in human breast cancer: Comparison with clinical variables and family history of cancer, ONCOL REP, 6(1), 1999, pp. 117-122
Replication error in colorectal carcinoma: Association with loss of heterozygosity at mismatch repair loci and clinicopathological variables
Authors: Johannsdottir, JT Bergthorsson, JT Gretarsdottir, S Kristjansson, AK Ragnarsson, G Jonasson, JG Egilsson, V Ingvarsson, S
Citation: Jt. Johannsdottir et al., Replication error in colorectal carcinoma: Association with loss of heterozygosity at mismatch repair loci and clinicopathological variables, ANTICANC R, 19(3A), 1999, pp. 1821-1826
Chromosome alterations and E-cadherin gene mutations in human lobular breast cancer
Authors: Huiping, C Sigurgeirsdottir, JR Jonasson, JG Eiriksdottir, G Johannsdottir, JT Egilsson, V Ingvarsson, S
Citation: C. Huiping et al., Chromosome alterations and E-cadherin gene mutations in human lobular breast cancer, BR J CANC, 81(7), 1999, pp. 1103-1110
Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival
Authors: Ragnarsson, G Eiriksdottir, G Johannsdottir, JT Jonasson, JG Egilsson, V Ingvarsson, S
Citation: G. Ragnarsson et al., Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival, BR J CANC, 79(9-10), 1999, pp. 1468-1474
Mapping lass of heterozygosity at chromosome 13q: Loss at 13q12-q13 is associated with breast tumour progression and poor prognosis
Authors: Eiriksdottir, G Johannesdottir, G Ingvarsson, S Bjornsdottir, IB Jonasson, JG Agnarsson, BA Hallgrimsson, J Gudmundsson, J Egilsson, V Sigurdsson, H Barkardottir, RB
Citation: G. Eiriksdottir et al., Mapping lass of heterozygosity at chromosome 13q: Loss at 13q12-q13 is associated with breast tumour progression and poor prognosis, EUR J CANC, 34(13), 1998, pp. 2076-2081
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