HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A

Georg Moessmer, Burkhardt Müller, Martin Kolben, Manfred Schmitt, Karl Theodor Maria Schneider, Almut Artmann

Research output: Contribution to journalArticlepeer-review

1 Scopus citations
Original languageEnglish
Pages (from-to)787-788
Number of pages2
JournalThrombosis and Haemostasis
Issue number4
StatePublished - Apr 2005
Externally publishedYes

Cite this