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

✍ Scribed by GÖRAN CARLSSON; MATS ANDERSSON; KATRIN PÜTSEP; DANIEL GARWICZ; MAGNUS NORDENSKJÖLD; JAN-INGE HENTER; JAN PALMBLAD; BENGT FADEEL


Book ID
114495316
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
344 KB
Volume
95
Category
Article
ISSN
0803-5253

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