Annika Mårtensson

affiliated with the university
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  1. 2016
  2. Origin of mutation in sporadic cases of severe haemophilia A in Sweden.

    Annika Mårtensson, Sten Ivarsson, Letelier, A., Manderstedt, E., Halldén, C. & Rolf Ljung, 2016, In : Clinical Genetics. 90, 1, p. 63-68

    Research output: Contribution to journalArticle

  3. 2015
  4. Haemophilia in Sweden – Studies on mutations and clinical implications

    Annika Mårtensson, 2015, Department of Paediatrics, Lund University. 78 p.

    Research output: ThesisDoctoral Thesis (compilation)

  5. Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.

    Annika Mårtensson, Letelier, A., Halldén, C. & Rolf Ljung, 2015, In : Haemophilia.

    Research output: Contribution to journalArticle

  6. 2014
  7. 2013
  8. Origin of Swedish hemophilia B mutations

    Hallden, C., Annika Mårtensson, Nilsson, D., Torbjörn Säll, Lind-Hallden, C., Liden, A. C. & Rolf Ljung, 2013, In : Journal of Thrombosis and Haemostasis. 11, 11, p. 2001-2008

    Research output: Contribution to journalArticle

  9. 2011
  10. Thirty-years' experience of prenatal diagnosis of haemophilia in Sweden

    R. Ljung & ANNIKA MÅRTENSSON, 2011 Jul 1, In : Journal of Thrombosis and Haemostasis. 9, p. 462 1 p., P-TU-492.

    Research output: Contribution to journalPublished meeting abstract