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2007
Mark Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities
Balciuniene, Jorune ; Feng, Ningping ; Iyadurai, Kelly ; Hirsch, Betsy ; Charnas, Lawrence ; Bill, Brent R. ; Easterday, Mathew C. ; Staaf, Johan ^LU ; Oseth, LeAnn and Czapansky-Beilman, Desiree , et al. (2007) In American Journal of Human Genetics 80(5). p.938-947
- Contribution to journal › Article
Mark Microarray analysis of gliomas reveals chromosomal position-associated gene expression patterns and identifies potential immunotherapy targets.
Persson, Oscar ^LU ; Krogh, Morten ^LU ; Saal, Lao ^LU ; Englund, Elisabet ^LU ; Liu, Jian ^LU ; Parsons, Ramon ; Mandahl, Nils ^LU ; Borg, Åke ^LU ; Widegren, Bengt ^LU and Salford, Leif ^LU (2007) In Journal of Neuro-Oncology 85(J1). p.11-24
- Contribution to journal › Article
2006
Mark Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities
Gustavsson, P ; Schoumans, J ; Staaf, Johan ^LU ; Jönsson, Göran B ^LU ; Carlsson, F ; Kristoffersson, Ulf ^LU ; Borg, Åke ^LU ; Nordenskjold, M and Dahl, N (2006) In Clinical Genetics 69(5). p.441-443
- Contribution to journal › Letter
Mark Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
Davidsson, Josef ^LU ; Heidenblad, Markus ^LU ; Borg, Åke ^LU and Johansson, Bertil ^LU (2006) In Cancer Genetics and Cytogenetics 169(2). p.179-180
- Contribution to journal › Letter
Mark Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies
Karppinen, S. -M. ; Barkardottir, R. B. ; Harbst, Katja ^LU ; Sydenham, T. ; Syrjakoski, K. ; Schleutker, J. ; Ikonen, T. ; Pylkas, K. ; Rapakko, K. and Erkko, H. , et al. (2006) In Journal of Medical Genetics 43(11). p.856-862
- Contribution to journal › Article
2005
Mark Classification of BRCA1 missense variants of unknown clinical significance
Phelan, C M ; Dapic, V ; Tice, B ; Favis, R ; Kwan, E ; Barany, F ; Manoukian, S ; Radice, P ; van der Luijt, R B and van Nesselrooij, B P M , et al. (2005) In Journal of Medical Genetics 42(2). p.138-146
- Contribution to journal › Article
Mark Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies
Antoniou, A C ; Pharoah, P D P ; Narod, S ; Risch, H A ; Eyfjord, J E ; Hopper, J L ; Olsson, Håkan ^LU ; Johannsson, O ; Borg, Åke ^LU and Pasini, B , et al. (2005) In Journal of Medical Genetics 42(7). p.602-603
- Contribution to journal › Article
2003
Mark Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
Antoniou, A ; Pharoah, PDP ; Narod, S ; Risch, HA ; Eyfjord, JE ; Hopper, JL ; Loman, Niklas ^LU ; Olsson, H ^LU ; Johannsson, O and Borg, Åke ^LU , et al. (2003) In American Journal of Human Genetics 72(5). p.1117-1130
- Contribution to journal › Article
Mark BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland
Perkowska, Magdalena ; BroZek, Izabela ; Wysocka, Barbara ; Haraldsson, Karin ^LU ; Törngren, Therese ^LU ; Johansson, Ulla ^LU ; Sellberg, Gunilla ^LU ; Borg, Åke ^LU and Limon, Janusz (2003) In Human Mutation 21(5). p.553-554
- Contribution to journal › Article
2002
Mark A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes
Rozenblum, E ; Vahteristo, P ; Törngren, Therese ^LU ; Bergthorsson, JT ; Syrjakoski, K ; Weaver, D ; Haraldsson, Karin ^LU ; Johannsdottir, HK ; Vehmanen, P and Nigam, S , et al. (2002) In Human Genetics 110(2). p.111-121
- Contribution to journal › Article

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