Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization-Reference-Cited by-同舟云学术

Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization

Published:2010-07-05 Issue:1 Volume:26 Page:136-143
ISSN:1460-2385
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:

Author:

Weber Stefanie,Landwehr Christina,Renkert Miriam,Hoischen Alexander,Wühl Elke,Denecke Jonas,Radlwimmer Bernhard,Haffner Dieter,Schaefer Franz,Weber Ruthild G.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/26/1/136/17107879/gfq400.pdf

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4. A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family;Abdelhak;Nat Genet,1997

5. Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease;Bingham;Am J Hum Genet,2001

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