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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis (sequence analysis of CD2AP gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Wilms tumor susceptibility-5, 601583, Autosomal dominant, Somatic mutation; WT5 (Nephroblastoma) (POU6F2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Wilms Tumor Panel

PreventionGenetics, part of Exact Sciences
United States
4828
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Wilms tumor: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
46
  • C Sequence analysis of the entire coding region

CEN4GEN Comprehensive Hereditary Cancer Syndrome: Gene sequencing Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1143
  • C Sequence analysis of the entire coding region

POU6F2 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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