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          Institute: MPI für Biochemie     Collection: Molecular Medicine (R. Fässler)     Display Documents



  history
ID: 226621.0, MPI für Biochemie / Molecular Medicine (R. Fässler)
New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene
Authors:Zerres, K.; Senderek, J.; Rudnik-Schoneborn, S.; Eggermann, T.; Kunze, J.; Mononen, T.; Kaariainen, H.; Kirfel, J.; Moser, M.; Buettner, R.; Bergmann, C.
Date of Publication (YYYY-MM-DD):2004
Title of Journal:Clinical Genetics
Volume:66
Start Page:53
End Page:57
Review Status:not specified
Audience:Not Specified
External Publication Status:published
Document Type:Article
Affiliations:MPI für Biochemie/Molecular Medicine (R. Fässler)/Research Group Moser
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