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

doi:10.1055/s-0037-1616784

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

Associate Professorship of Nephrology

Technical University of Munich

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Original language	English
Pages (from-to)	787-788
Number of pages	2
Journal	Thrombosis and Haemostasis
Volume	93
Issue number	4
DOIs	https://doi.org/10.1055/s-0037-1616784
State	Published - Apr 2005

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

author = "Georg Moessmer and Burkhardt M{\"u}ller and Martin Kolben and Manfred Schmitt and Schneider, {Karl Theodor Maria} and Almut Artmann",

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AU - Müller, Burkhardt

AU - Kolben, Martin

AU - Schmitt, Manfred

AU - Schneider, Karl Theodor Maria

AU - Artmann, Almut

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

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