New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene-Reference-Cited by-同舟云学术

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

Published:2004-06-16 Issue:1 Volume:66 Page:53-57
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Zerres K,Senderek J,Rudnik-Schöneborn S,Eggermann T,Kunze J,Mononen T,Kääriäinen H,Kirfel J,Moser M,Buettner R,Bergmann C

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Autosomal recessive polycystic kidney disease. Problems of prenatal diagnosis;Zerres;Prenat Diagn,1988

2. Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen;Zerres;Nat Genet,1994

3. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology;Zerres;Am J Med,1998

4. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein;Ward;Nat Genet,2002

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