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Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences. Klinisk kemi och farmakologi. (Inflammation)
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2006 (English)In: Acta Paediatrica, ISSN 0803-5253, E-ISSN 1651-2227, Vol. 95, no 12, 1526-32 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2006. Vol. 95, no 12, 1526-32 p.
Keyword [en]
Agranulocytosis/genetics/*history/physiopathology, History; 20th Century, Humans, Neutropenia/congenital/*history, Portraits as Topic, Sweden
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URN: urn:nbn:se:uu:diva-17302PubMedID: 17129957OAI: oai:DiVA.org:uu-17302DiVA: diva2:45073
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Publikation från annat universitet

Available from: 2008-06-19 Created: 2008-06-19 Last updated: 2017-12-08

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Garwicz, Daniel

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