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          Document History for Document ID 221576

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Document Version Version Comment Date Status
221576.0 [No comment] 17.06.2005 09:16 Released

ID: 221576.0, MPI für Biochemie / Molecular Medicine (R. Fässler)
PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)
Authors:Bergmann, C.; Senderek, J.; Schneider, F.; Dornia, C.; Kupper, F.; Eggermann, T.; Rudnik-Schöneborn, S.; Kirfel, J.; Moser, M.; Büttner, R.; Zerres, K.
Language:English
Date of Publication (YYYY-MM-DD):2004
Title of Journal:Human Mutation
Journal Abbrev.:Hum. Mutat.
Volume:23
Issue / Number:5
Start Page:487
End Page:495
Review Status:Peer-review
Audience:Not Specified
Free Keywords:autosomal recessive polycystic kidney disease; ARPKD; polycystic kidney and hepatic disease 1; PKHD1; fibrocystin; polyductin; mutation analysis; genotype-phenotype correlation; prenatal diagnosis
External Publication Status:published
Document Type:Article
Affiliations:MPI für Biochemie/Molecular Medicine (R. Fässler)/Research Group Moser
External Affiliations:Univ Aachen, Dept Human Genet, D-52074 Aachen, Germany.; Univ Bonn, Dept Pathol, D-5300 Bonn, Germany.
Identifiers:ISI:000221119500012 [ID No:1]
ISSN:1059-7794 [ID No:2]