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Maternal factor V Leiden and prothrombin mutations do not seem to contribute to the occurrence of two or more than two consecutive miscarriages in Caucasian patients

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Background: We analysed the prevalence of the most common hereditary thrombophilia (hTP) - factor V Leiden (FVL) mutation, prothrombin 20210 G>A substitution (PT) - and the 677 C>T replacement in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in Caucasian patients with a history of...

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Main Authors: Baumann, Kristin (Author) , Beuter-Winkler, Petra (Author) , Hackethal, Andreas (Author) , Strowitzki, Thomas (Author) , Toth, Bettina (Author) , Bohlmann, Michael K. (Author)
Format: Article (Journal)
Language:English
Published: 25 June 2013
In: American journal of reproductive immunology
Year: 2013, Volume: 70, Issue: 6, Pages: 518-521
ISSN:1600-0897
DOI:10.1111/aji.12144
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1111/aji.12144
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/aji.12144
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Author Notes:Kristin Baumann, Petra Beuter‐Winkler, Andreas Hackethal, Thomas Strowitzki, Bettina Toth, Michael K. Bohlmann
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Maternal factor V Leiden and prothrombin mutations do not seem to contribute to the occurrence of two or more than two consecutive miscarriages in Caucasian patients by Baumann, Kristin (Author) , Beuter-Winkler, Petra (Author) , Hackethal, Andreas (Author) , Strowitzki, Thomas (Author) , Toth, Bettina (Author) , Bohlmann, Michael K. (Author) ,


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