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

Document type:: Case Reports; Journal Article; Article
Author(s):: Moessmer, G; Müller, B; Kolben, M; Schmitt, M; Schneider, KT; Artmann, A
Title:: HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A.
Journal title abbreviation:: Thromb Haemost
Year:: 2005
Journal volume:: 93
Journal issue:: 4
Pages contribution:: 787-8
Language:: eng
Fulltext / DOI:: doi:10.1267/THRO05040787
Pubmed ID:: http://view.ncbi.nlm.nih.gov/pubmed/15841328
Print-ISSN:: 0340-6245
TUM Institution:: Fachgebiet Perinatalmedizin und Perinatalphysiologie (Prof. Schneider); Frauenklinik und Poliklinik; Institut für Klinische Chemie und Pathobiochemie
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