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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

Targeted Oncology Microarray Analysis

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
77
  • D Deletion/duplication analysis

Wilms tumor 2, 194071, Autosomal dominant, Somatic mutation; WT2 (Nephroblastoma) (H19 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 2, 194071, Autosomal dominant, Somatic mutation; WT2 (Nephroblastoma) (H19 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Beckwith-Wiedemann syndrome panel

Genologica Medica
Spain
2010
  • C Sequence analysis of the entire coding region

Beckwith-Wiedemann syndrome panel. NGS panel of 10 genes.

Genologica Medica
Spain
2010
  • 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

H19 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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