Search Results

Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden

by Melin, M., Entesarian, M., Carlsson, G., Garwicz, D., Klein, C., Fadeel, B., Nordenskjöld, M., Palmblad, J., Henter, J.I., Dahl, N.
Published in Biochemical and Biophysical Research Communications (2007)

Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations

by Carlsson, G., Van’t Hooft, I., Melin, M., Entesarian, M., Laurencikas, E., Nennesmo, I., Trębińska, A., Grzybowska, E., Palmblad, J., Dahl, N., Nordenskjöld, M., Fadeel, B., Henter, J‐I
Published in Journal of Internal Medicine (2008)