Larsen, Christopher P <br/><br/>
Fluorescence in situ hybridization for the diagnosis of NPHP1 deletion-related nephronophthisis on renal biopsy.  [electronic resource] 

 -  Human pathology  11 2018 
 - 71-77 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1532-8392 
<br/><br/><label>Standard No.: </label>10.1016/j.humpath.2018.06.021  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing--genetics<br/>Adolescent<br/>Adult<br/>Biopsy<br/>Child<br/>Child, Preschool<br/>Cytoskeletal Proteins<br/>Female<br/>Gene Deletion<br/>Genetic Markers<br/>Genetic Predisposition to Disease<br/>Homozygote<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Kidney--pathology<br/>Kidney Diseases, Cystic--complications<br/>Male<br/>Membrane Proteins--genetics<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Predictive Value of Tests<br/>Renal Insufficiency, Chronic--genetics<br/>Risk Factors<br/>Young Adult