CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)-Reference-Cited by-同舟云学术

CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)

Published:2011-12-06 Issue:6 Volume:27 Page:2355-2364
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Brockschmidt A.,Chung B.,Weber S.,Fischer D.-C.,Kolatsi-Joannou M.,Christ L.,Heimbach A.,Shtiza D.,Klaus G.,Simonetti G. D.,Konrad M.,Winyard P.,Haffner D.,Schaefer F.,Weber R. G.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/27/6/2355/6905365/gfr649.pdf

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5. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

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