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2016
Mark Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia
Ivanov Öfverholm, Ingegerd ; Tran, Anh Nhi ; Olsson, Linda ^LU ; Zachariadis, Vasilios ; Heyman, Mats ; Rudd, Eva ; Syk Lundberg, Elisabeth ; Nordenskjöld, Magnus ; Johansson, Bertil ^LU and Nordgren, Ann , et al. (2016) In Leukemia & Lymphoma 57(9). p.2161-2170
- Contribution to journal › Article
2013
Mark Transformation of a plasmid-free, genital tract isolate of Chlamydia trachomatis with a plasmid vector carrying a deletion in CDS6 revealed that this gene regulates inclusion phenotype
Wang, Yibing ; Cutcliffe, Lesley T. ; Skilton, Rachel J. ; Persson, Kenneth ^LU ; Bjartling, Carina ^LU and Clarke, Ian N. (2013) In Pathogens and Disease 67(2). p.100-103
- Contribution to journal › Article
2011
Mark Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation
Gilling, Mette ; Lind-Thomsen, Allan ; Mang, Yuan ; Bak, Mads ; Moller, Morten ; Ullmann, Reinhard ; Kristoffersson, Ulf ^LU ; Kalscheuer, Vera M. ; Henriksen, Karen Friis and Bugge, Merete , et al. (2011) In European Journal of Medical Genetics 54(4). p.383-388
- Contribution to journal › Article
2009
Mark Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
Depienne, Christel ; Moreno-De-Luca, Daniel ; Heron, Delphine ; Bouteiller, Delphine ; Gennetier, Aurélie ; Delorme, Richard ; Chaste, Pauline ; Siffroi, Jean-Pierre ; Chantot-Bastaraud, Sandra and Benyahia, Baya , et al. (2009) In Biological Psychiatry 66(4). p.349-359
- Contribution to journal › Article
2008
Mark The effect of pedigree structure on detection of deletions and other null alleles.
Johansson, Anna ^LU and Säll, Torbjörn ^LU (2008) In European Journal of Human Genetics 16(10). p.1225-1234
- Contribution to journal › Article
Mark CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome
Wincent, J ; Holmberg, E ; Stromland, K ; Soller, Maria ^LU ; Mirzaei, L ; Djureinovic, T ; Robinson, K L ; Anderlid, B M and Schoumans, J (2008) In Clinical Genetics 74(1). p.31-38
- Contribution to journal › Article
2007
Mark Detecting Deletions by Analysis of Genetic Markers in Pedigrees
Johansson, Anna ^LU (2007)
- Thesis › Doctoral thesis (compilation)
2005
Mark The 5 ' Region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences
Charbonnier, FC ; Baert-Desurmont, S ; Liang, P ; Di Fiore, F ; Martin, C ; Frerot, S ; Olschwang, S ; Wang, Q ; Buisine, MP and Gilbert, B , et al. (2005) In Human Mutation 26(3). p.255-261
- Contribution to journal › Article
Mark Large deletions of the PROS1 gene in a large fraction of mutationnegative patients with protein S deficiency
Johansson, Anna ^LU ; Hillarp, Andreas ^LU ; Säll, Torbjörn ^LU ; Zöller, Bengt ^LU ; Dahlbäck, Björn ^LU and Halldén, Christer ^LU (2005) In Thrombosis and Haemostasis 94(5). p.951-957
- Contribution to journal › Article
2002
Mark Uneven distribution of repetitive trinucleotide motifs in human immunoglobulin heavy variable genes
Lantto, Johan ^LU and Ohlin, Mats ^LU (2002) In Journal of Molecular Evolution 54(3). p.346-353
- Contribution to journal › Article

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