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 - Moessmer, Georg

AU - Müller, Burkhardt

AU - Kolben, Martin

AU - Schmitt, Manfred

AU - Schneider, Karl Theodor Maria

AU - Artmann, Almut

PY - 2005/4

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JO - Thrombosis and Haemostasis

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IS - 4

ER -

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

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