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Klinische Padiatrie|April 20, 2012
Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 familiesK Sandrock, S Halimeh, V Wiegering, et al.
Klinische Padiatrie|November 1, 1990
[Fanconi-Bickel syndrome]H C Koch, R Mallmann
Klinische Padiatrie|November 1, 1990
[Hemophagocytic syndrome in childhood]K M Lücking-Famira, B Kumlien, W Permanetter, et al.
Klinische Padiatrie|January 1, 1989
[Coronary aneurysm in Kawasaki syndrome: incidence and prognosis]A Beitzke, G Zobel
Klinische Padiatrie|November 1, 1977
[Acute hemorrhagic meningoencephalitis due to rubella-infection in acute lymphatic leukemia (author's transl)]R Korinthenberg, H Breu, D Palm, et al.
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