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2013
Mark Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
Hemminki, Kari ^LU ; Li, Xinjun ^LU ; Försti, Asta ^LU ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2013) In BMC Medical Genetics 14.
- Contribution to journal › Article
Mark Investigating highly replicated asthma genes as candidate genes for allergic rhinitis
Andiappan, Anand Kumar ; Nilsson, Daniel ; Hallden, Christer ; De Yun, Wang ; Säll, Torbjörn ^LU ; Cardell, Lars Olaf and Tim, Chew Fook (2013) In BMC Medical Genetics 14.
- Contribution to journal › Article
2012
Mark The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmo Diet and cancer study
Fava, Cristiano ^LU ; Montagnana, Martina ^LU ; Danese, Elisa ; Sjögren, Marketa ^LU ; Almgren, Peter ^LU ; Engström, Gunnar ^LU ; Hedblad, Bo ^LU ; Guidi, Gian Cesare ; Minuz, Pietro and Melander, Olle ^LU (2012) In BMC Medical Genetics 13.
- Contribution to journal › Article
Mark Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer
Lascorz, Jesus ; Bevier, Melanie ; Schoenfels, Witigo V. ; Kalthoff, Holger ; Aselmann, Heiko ; Beckmann, Jan ; Egberts, Jan ; Buch, Stephan ; Becker, Thomas and Schreiber, Stefan , et al. (2012) In BMC Medical Genetics 13.
- Contribution to journal › Article
Mark Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
Huhn, Stefanie ; Bevier, Melanie ; Rudolph, Anja ; Pardini, Barbara ; Naccarati, Alessio ; Hein, Rebecca ; Hoffmeister, Michael ; Vodickova, Ludmila ; Novotny, Jan and Brenner, Hermann , et al. (2012) In BMC Medical Genetics 13(94).
- Contribution to journal › Article
Mark Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study
Nilsson, Daniel ; Andiappan, Anand Kumar ; Halldén, Christer ^LU ; Yun, Wang De ; Säll, Torbjörn ^LU ; Tim, Chew Fook and Cardell, Lars-Olaf (2012) In BMC Medical Genetics 13(66).
- Contribution to journal › Article
2011
Mark A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study
Roshandel, Delnaz ; Thomson, Wendy ; Pye, Stephen R. ; Boonen, Steven ; Borghs, Herman ; Vanderschueren, Dirk ; Huhtaniemi, Ilpo T. ; Adams, Judith E. ; Ward, Kate A. and Bartfai, Gyorgy , et al. (2011) In BMC Medical Genetics 12.
- Contribution to journal › Article
2009
Mark An investigation of ribosomal protein L10 gene in autism spectrum disorders
Gong, Xiaohong ; Delorme, Richard ; Fauchereau, Fabien ; Durand, Christelle M ; Chaste, Pauline ; Betancur, Catalina ; Goubran-Botros, Hany ; Nygren, Gudrun ; Anckarsäter, Henrik ^LU and Råstam, Maria ^LU , et al. (2009) In BMC Medical Genetics 10(7).
- Contribution to journal › Article
Mark Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels
Bartuma, Katarina ^LU ; Carlsson, Christina ^LU ; Bendahl, Pär-Ola ^LU and Nilbert, Mef ^LU (2009) In BMC Medical Genetics 10.
- Contribution to journal › Article
2008
Mark Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
Davidsson, Josef ^LU ; Collin, Anna ^LU ; Björkhem, Gudrun ^LU and Soller, Maria ^LU (2008) In BMC Medical Genetics 9(2).
- Contribution to journal › Article

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