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1997
Mark The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer : a population-based cohort study
Bratt, O ^LU ; Kristoffersson, U ^LU ; Lundgren, R and Olsson, Håkan ^LU (1997) In European Journal of Cancer 33(13). p.2237-2240
- Contribution to journal › Article
Mark von Willebrand factor mediates increased platelet retention in recurrent thrombotic thrombocytopenic purpura
Karpman, D ^LU ; Lethagen, S ^LU ; Kristoffersson, Anne ^LU ; Isaksson, C. and Holmberg, Lars ^LU (1997) In Thrombosis and Haemostasis 78(6). p.62-1456
- Contribution to journal › Article
1996
Mark A novel p53 germline alteration identified in a late onset breast cancer kindred
Sun, X F ; Johannsson, O ^LU ; Håkansson, S ; Sellberg, G ^LU ; Nordenskjöld, B ; Olsson, H ^LU and Borg, A ^LU (1996) In Oncogene 13(2). p.11-407
- Contribution to journal › Article
Mark Novel germline p16 mutation in familial malignant melanoma in southern Sweden
Borg, Åke ^LU ; Johannsson, U ; Johannsson, O ^LU ; Hakansson, Sara ; Westerdahl, J ^LU ; Mäsbäck, A ^LU ; Olsson, Håkan ^LU and Ingvar, C ^LU (1996) In Cancer Research 56(11). p.500-2497
- Contribution to journal › Article
Mark Familial testicular cancer in Norway and southern Sweden
Heimdal, K ; Olsson, Håkan ^LU ; Tretli, S ; Flodgren, P ^LU ; Børresen, A L and Fossa, S D (1996) In British Journal of Cancer 73(7). p.9-964
- Contribution to journal › Article
1995
Mark A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study
Cogan, J D ; Ramel, B ^LU ; Lehto, M ; Phillips, J ; Prince, M ; Blizzard, R M ; de Ravel, T J ; Brammert, M and Groop, L ^LU (1995) In The Journal of clinical endocrinology and metabolism 80(12). p.5-3591
- Contribution to journal › Article
1993
Mark Haemophilia : strategies for carrier detection and prenatal diagnosis
Peake, I R ; Lillicrap, D P ; Boulyjenkov, V ; Briet, E ; Chan, V ; Ginter, E K ; Kraus, E M ; Ljung, R ^LU ; Mannucci, P M and Nicolaides, K (1993) In Bulletin of the World Health Organization 71(3-4). p.58-429
- Contribution to journal › Article
1990
Mark Two factor IX mutations in the family of an isolated haemophilia B patient : direct carrier diagnosis by amplification mismatch detection (AMD)
Montandon, A J ; Green, P M ; Bentley, D R ; Ljung, R ^LU ; Nilsson, Inga Marie and Giannelli, F (1990) In Human Genetics 85(2). p.4-200
- Contribution to journal › Article
1987
Mark Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage
Jensson, O ; Gudmundsson, G ; Arnason, A ; Blöndal, H ; Petursdottir, I ; Thorsteinsson, L ; Grubb, A ^LU ; Löfberg, H ^LU ; Cohen, D and Frangione, B (1987) In Acta Neurologica Scandinavica 76(2). p.102-114
- Contribution to journal › Article
1982
Mark Genetic variants of haemophilia B detected by immunoradiometric assay : implications for prenatal diagnosis
Ljung, R ^LU and Holmberg, Lars ^LU (1982) In Pediatric Research 16(3). p.8-256
- Contribution to journal › Article

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