Lehnhardt, Anja <br/><br/>
Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.  [electronic resource] 

 -  Clinical journal of the American Society of Nephrology : CJASN  May 2015 
 - 825-31 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1555-905X 
<br/><br/><label>Standard No.: </label>10.2215/CJN.10141014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Austria<br/>Child<br/>Child, Preschool<br/>Exons--genetics<br/>Female<br/>Genes, Wilms Tumor<br/>Germany<br/>Heterozygote<br/>Humans<br/>Infant<br/>Introns--genetics<br/>Karyotype<br/>Kidney Diseases--genetics<br/>Kidney Neoplasms--diagnosis<br/>Kidney Transplantation<br/>Male<br/>Mutation, Missense<br/>Nephrectomy<br/>Phenotype<br/>Proteinuria--diagnosis<br/>Renal Dialysis<br/>Retrospective Studies<br/>Switzerland<br/>Urogenital Abnormalities--genetics<br/>Wilms Tumor--diagnosis<br/>Young Adult