Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia.

MLA

Carlsson, Göran, et al. “Kostmann Syndrome or Infantile Genetic Agranulocytosis, Part One: Celebrating 50 Years of Clinical and Basic Research on Severe Congenital Neutropenia.” Acta Paediatrica, vol. 95, no. 12, Dec. 2006, pp. 1526–32. EBSCOhost, https://doi.org/10.1080/08035250601087607.

APA

Carlsson, G., Andersson, M., Pütsep, K., Garwicz, D., Nordenskjöld, M., Henter, J.-I., Palmblad, J., Fadeel, B., Carlsson, G., Pütsep, K., & Nordenskjöld, M. (2006). Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia. Acta Paediatrica, 95(12), 1526–1532. https://doi.org/10.1080/08035250601087607

Chicago

Carlsson, Göran, Mats Andersson, Katrin Pütsep, Daniel Garwicz, Magnus Nordenskjöld, Jan-Inge Henter, Jan Palmblad, et al. 2006. “Kostmann Syndrome or Infantile Genetic Agranulocytosis, Part One: Celebrating 50 Years of Clinical and Basic Research on Severe Congenital Neutropenia.” Acta Paediatrica 95 (12): 1526–32. doi:10.1080/08035250601087607.