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2021
Mark Genetic Screening in Patients Suspected of Inherited Bleeding Disorders
Fager Ferrari, Marcus ^LU (2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
2017
Mark Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations
Ajore, Ram ^LU ; Raiser, David ; McConkey, Marie E. ; Jöud, Magnus ^LU ; Boidol, Bernd ; Mar, Brenton G ; Saksena, Gordon ; Weinstock, David M ; Armstrong, Scott and Ellis, Steven R , et al. (2017) In EMBO Molecular Medicine 9(4). p.498-507
- Contribution to journal › Article
2016
Mark 'It made you think twice' - an interview study of women's perception of a web-based decision aid concerning screening and diagnostic testing for fetal anomalies
Åhman, Annika ; Sarkadi, Anna ; Lindgren, Peter and Rubertsson, Christine ^LU (2016) In BMC Pregnancy and Childbirth 16(1).
- Contribution to journal › Article
2015
Mark Risk Screening, Testing, and Diagnosis : Ethical Aspects
Hermerén, Göran ^LU (2015) p.698-705
- Chapter in Book/Report/Conference proceeding › Book chapter
2014
Mark Neuroacanthocytosis - Clinical variability (a report on six cases)
Dulski, J. ; Soltan, W. ; Schinwelski, M. ; Sitek, E. J. ; Rudzinska, Monika ; Wójcik-Pedziwiatr, M. ; Wictor, L. ^LU ; Schön, F. ; Puschmann, A. ^LU and Klempir, J. , et al. (2014) Eighteenth International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 29(Suppl 1). p.194-194
- Contribution to journal › Published meeting abstract
2008
Mark EuroGentest: DNA-based testing for heritable disorders in Europe
Javahera, Poupak ; Kaariainen, Helena ; Kristoffersson, Ulf ^LU ; Nippert, Irmgard ; Sequeiros, Jorge ; Zirnmern, Ron and Schmidtke, Joerg (2008) In Community Genetics 11(2). p.75-120
- Contribution to journal › Article
2007
Mark Malignant hyperthermia and central core disease causative mutations in Swedish patients.
Broman, M ; Islander, Gunilla ^LU ; Muller, C R and Ranklev Twetman, Eva ^LU (2007) In Acta Anaesthesiologica Scandinavica 51(Nov 1). p.50-53
- Contribution to journal › Article
2004
Mark BRCA1 och BRCA2 har nått kliniken. Tioårigt fynd av genmutation ger nu möjlighet förebygga ärftlig bröstcan
Loman, Niklas ^LU (2004) In Läkartidningen 101(25). p.7-2172
- Contribution to journal › Article
2002
Mark Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
Lindgren, Cecilia ^LU ; Widén, Elisabeth ; Tuomi, Tiinamaija ^LU ; Li, Haiyan ^LU ; Almgren, Peter ^LU ; Kanninen, Timo ; Melander, Olle ^LU ; Weng, Jianping ; Lehto, Markku and Groop, Leif ^LU (2002) In Diabetes 51(5). p.1609-1617
- Contribution to journal › Article
1999
Mark Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: Comparison with a control group
Tedgård, U. ^LU ; Ljung, R. ^LU and McNeil, T.F. ^LU (1999) In Prenatal Diagnosis 19(5). p.411-417
- Contribution to journal › Article

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