Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Human Heredity|August 25, 2005
Detecting deletions in families affected by a dominant disease by use of marker dataAnna M Johansson, Christer Halldén, Torbjorn Sall
Annals of Human Genetics|May 4, 2011
Variation in the VWF gene in Swedish patients with type 1 von Willebrand DiseaseAnna M Johansson, Christer Halldén, Torbjörn Säll, et al.
Respiratory Investigation|June 11, 2025
Rare-variant collapsing analyses of asthma in the UK biobankBengt Zöller, Eric Manderstedt, Christina Lind-Halldén, et al.
TH Open : Companion Journal to Thrombosis and Haemostasis|November 4, 2020
Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease PatientsEric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, et al.
TH Open : Companion Journal to Thrombosis and Haemostasis|June 29, 2019
Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease PatientsEric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, et al.
Journal of Thrombosis and Haemostasis : JTH|January 7, 2026
Non-carrier mothers of hemophilia A patients with Inv22 inversions often have other rearrangementsEric Manderstedt, Christina Lind-Halldén, Christer Halldén, et al.
Hereditas|February 11, 2005
Mode of reproduction in Arabidopsis suecicaTorbjörn Säll, Christina Lind-Halldén, Mattias Jakobsson, et al.
Plos One|February 2, 2018
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patientsEric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 24, 2006
Evolution of chloroplast mononucleotide microsatellites in Arabidopsis thalianaMattias Jakobsson, Torbjörn Säll, Christina Lind-Halldén, et al.
Pageof 5