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2008
Mark Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis : the GENOMOS study
Langdahl, Bente L ; Uitterlinden, André G ; Ralston, Stuart H ; Trikalinos, Thomas A ; Balcells, Susanne ; Brandi, Maria Luisa ; Scollen, Serena ; Lips, Paul ; Lorenc, Roman and Obermayer-Pietsch, Barbara , et al. (2008) In Bone 42(5). p.81-969
- Contribution to journal › Article
2005
Mark Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone
Albagha, O M E ; Pettersson, U ; Stewart, A ; McGuigan, F E A ^LU ; MacDonald, H M ; Reid, D M and Ralston, S H (2005) In Journal of Medical Genetics 42(3). p.6-240
- Contribution to journal › Article
Mark Polymorphisms of the CLCN7 gene are associated with BMD in women
Pettersson, Ulrika ; Albagha, Omar M E ; Mirolo, Max ; Taranta, Anna ; Frattini, Annalisa ; McGuigan, Fiona E A ^LU ; Vezzoni, Paolo ; Teti, Anna ; van Hul, Wim and Reid, David M , et al. (2005) In Journal of Bone and Mineral Research 20(11). p.7-1960
- Contribution to journal › Article
2004
Mark Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes
Doney, A S F ; Fischer, B ; Cecil, J E ; Boylan, K ; McGuigan, F E ^LU ; Ralston, S H ; Morris, A D and Palmer, C N A (2004) In Diabetologia 47(3). p.555-558
- Contribution to journal › Article
2002
Mark HLA-DQ genotypes in classic type 1 diabetes and in latent autoimmune diabetes of the adult.
Stenström, Gunnar ; Berger, Bo ; Borg, Henrik ^LU ; Fernlund, Per ^LU ; Dorman, Janice S and Sundkvist, Göran (2002) In American Journal of Epidemiology 156(9). p.787-796
- Contribution to journal › Article
2001
Mark Effect of a COL1A1 Sp1 binding site polymorphism on arterial pulse wave velocity : an index of compliance
Brull, D J ; Murray, L J ; Boreham, C A ; Ralston, S H ; Montgomery, H E ; Gallagher, A M ; McGuigan, F E ^LU ; Davey Smith, G ; Savage, M and Humphries, S E , et al. (2001) In Hypertension 38(3). p.8-444
- Contribution to journal › Article
Mark The NciI polymorphism in the cyclin D1 gene and sporadic primary hyperparathyroidism
Correa, P ^LU ; Lundgren, E ; Rastad, J ; Akerström, G ; Westin, G and Carling, T (2001) In Journal of Internal Medicine 250(6). p.20-516
- Contribution to journal › Article
2000
Mark Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion
Larsson, J ; Hultberg, B ^LU and Hillarp, A ^LU (2000) In Acta Ophthalmologica Scandinavica 78(3). p.3-340
- Contribution to journal › Article
Mark Absence of cystatin C mutation in sporadic cerebral amyloid angiopathy-related hemorrhage
McCarron, M O ; Nicoll, J A ; Stewart, J ; Ironside, J W ; Mann, D M ; Love, S ; Graham, D I and Grubb, A ^LU (2000) In Neurology 54(1). p.242-244
- Contribution to journal › Article
1999
Mark The Ala25-Thr mutation in the thrombomodulin gene is not frequent in Swedish patients suffering from ischemic heart disease [9]
Norlund, Lena ^LU ; Holm, J. ^LU ; Zöller, Bengt ^LU and Öhlin, Ann-Kristin ^LU (1999) In Thrombosis and Haemostasis 82(4). p.1367-1368
- Contribution to journal › Letter

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