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Genomic Methods in the Diagnosis and Treatment of Pediatric Kidney Disease

Reference work entry

Abstract

The completion of the Human Genome Project (HGP) in 2003 has laid the foundation and driven the technological advancements necessary for the study of the genetics of complex, multifactorial diseases, such as those affecting the kidney. The International HapMap Project has built upon the HGP through the systematic identification and cataloging of genetic variation across human populations. Translating the mass of data generated by these studies into useful clinical knowledge is now a major undertaking in nearly all areas of medicine, including the field of pediatric nephrology. Much of this work will revolve around linking particular patient phenotypes to genomic and proteomic data, such as genotype, expression profile, and protein biomarkers

Keywords

Chronic Kidney Disease Nephrotic Syndrome Hemolytic Uremic Syndrome Human Genome Project Pediatric Nephrology 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2016

Authors and Affiliations

  1. 1.Section of Genomic PediatricsMedical College of WisconsinMilwaukeeUSA
  2. 2.Department of PediatricsMedical College of Wisconsin and Children’s Hospital of WisconsinMilwaukeeUSA

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