Search Results - Sjörin, E.

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  1. 1
    Investigation of disease-associated factors in haemophilia A patients without detectable mutations

    Investigation of disease-associated factors in haemophilia A patients without detectable mutations by HALLDÉN, C., KNOBE, K. E., SJÖRIN, E., NILSSON, D., LJUNG, R.

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  2. 2
    Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families?

    Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families? by KNOBE, K. E., SJÖRIN, E., LJUNG, R. C. R.

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  3. 3
    Functional analysis of the EGF‐like domain mutations Pro55Ser and Pro55Leu, which cause mild hemophilia B

    Functional analysis of the EGF‐like domain mutations Pro55Ser and Pro55Leu, which cause mild hemophilia B by Knobe, K. E., Persson, K. E. M., Sjörin, E., Villoutreix, B. O., Stenflo, J., Ljung, R. C. R.

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  4. 4
    Female haemophilia A caused by skewed X inactivation

    Female haemophilia A caused by skewed X inactivation by KNOBE, K. E., SJÖRIN, E., SOLLER, M. J., LILJEBJÖRN, H., LJUNG, R. C. R.

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  5. 5
    Haemophilia B mutations in Sweden: a population‐based study of mutational heterogeneity

    Haemophilia B mutations in Sweden: a population‐based study of mutational heterogeneity by Ljung, Rolf, Petrini, Pia, Tengborn, Lilian, Sjörin, Elsy

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  6. 6
    Origin of mutation in sporadic cases of haemophilia A

    Origin of mutation in sporadic cases of haemophilia A by Ljung, Rolf C. R., Sjörin, Elsy

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  7. 7
    Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A

    Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A by Kling, S, Ljung, R, Sjörin, E, Nilsson, I M

    Published in Human genetics
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  8. 8
    Inhibitors in the Swedish population with severe haemophilia A and B: a 20-year survey

    Inhibitors in the Swedish population with severe haemophilia A and B: a 20-year survey by Knobe, KE, Sjörin, E, Tengborn, LI, Petrini, P, Ljung, RCR

    Published in Acta Paediatrica
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  9. 9
    Female haemophilia A caused by skewed X inactivation

    Female haemophilia A caused by skewed X inactivation by Knobe, K E, Sjörin, E, Soller, M J, Liljebjörn, H, Ljung, R C R

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  10. 10
    Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A

    Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A by Kling, S, Ljung, R, Sjörin, E, Nilsson, I M

    Published in Human genetics
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