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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
Document Type: Article
ID: 226621.0
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