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Results: 1 to 10 of 10

Tests names and labsConditionsGenes, analytes, and microbesMethods

Long QT syndrome, acquired, reduced susceptibility to, 613688, Autosomal dominant (Familial long QT syndrome) (ALG10 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

WES metabolic disorders

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
1625
  • E Sequence analysis of select exons

Long QT syndrome (WES based NGS panel of 18 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
118
  • C Sequence analysis of the entire coding region

Cardiac conduction changes (WES based NGS panel of 29 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
129
  • C Sequence analysis of the entire coding region

Sudden death (WES based NGS panel of 80 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
180
  • C Sequence analysis of the entire coding region

SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1394
  • E Sequence analysis of select exons

HEREDITARY ARRHYTHMIA EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1160
  • E Sequence analysis of select exons

Long QT Syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1816
  • C Sequence analysis of the entire coding region

ALG10 Single Gene

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

ALG10B Single Gene

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

Results: 1 to 10 of 10

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