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New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene

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http://pubman.mpdl.mpg.de/cone/persons/resource/persons78420

Moser,  M.
Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society;

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Zerres, K., Senderek, J., Rudnik-Schoneborn, S., Eggermann, T., Kunze, J., Mononen, T., et al. (2004). New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene. Clinical Genetics, 66, 53-57.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0010-6A96-F
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