![](/img/cover-not-exists.png)
HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A
Moessmer, Georg, Müller, Burkhardt, Kolben, Martin, Schmitt, Manfred, Maria Schneider, Karl Theodor, Artmann, AlmutVolume:
93
Year:
2005
Language:
english
Journal:
Thrombosis and Haemostasis
DOI:
10.1055/s-0037-1616784
File:
PDF, 124 KB
english, 2005