Anna Johansson (Former)

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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
2007
Mark Detecting Deletions by Analysis of Genetic Markers in Pedigrees
Johansson, Anna ^LU (2007)
- Thesis › Doctoral thesis (compilation)
2005
Mark Detecting Deletions in Families Affected by a Dominant Disease by Use of Marker Data.
Johansson, Anna ^LU ; Halldén, Christer ^LU and Säll, Torbjörn ^LU (2005) In Human Heredity 60(1). p.26-35
- Contribution to journal › Article
Mark Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype.
Lanke, Elsa ^LU ; Johansson, Anna ^LU ; Halldén, Christer ^LU and Lethagen, Stefan ^LU (2005) In Journal of Thrombosis and Haemostasis 3(12). p.2656-2663
- 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
2004
Mark Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.
Lanke, Elsa ^LU ; Johansson, Anna ^LU ; Hillarp, Andreas ^LU ; Lethagen, Stefan ^LU ; Zöller, Bengt ^LU ; Dahlbäck, Björn ^LU and Halldén, Christer ^LU (2004) In Journal of Thrombosis and Haemostasis 2(11). p.1918-1923
- Contribution to journal › Article