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Title:

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
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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