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

Zerres, K.; Senderek, J.; Rudnik-Schoneborn, S.; Eggermann, T.; Kunze, J.; Mononen, T.; Kaariainen, H.; Kirfel, J.; Moser, M.; Buettner, R.; Bergmann, C.

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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-6A96-F Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-6A97-D

Genre: Journal Article

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Creators:
Zerres, K., Author
Senderek, J., Author
Rudnik-Schoneborn, S., Author
Eggermann, T., Author
Kunze, J., Author
Mononen, T., Author
Kaariainen, H., Author
Kirfel, J., Author
Moser, M.¹, Author
Buettner, R.², Author
Bergmann, C., Author

Affiliations:
1Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565147
2External Organizations, ou_persistent22

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Dates: Date issued: 2004

Publication Status: Issued

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Identifiers: eDoc: 226621

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Title: Clinical Genetics

Source Genre: Journal

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Pages: - Volume / Issue: 66 Sequence Number: - Start / End Page: 53 - 57 Identifier: -