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Results: 1 to 9 of 9 (representing 8 labs)

Tests names and labsConditionsGenes and analytesMethods

Dopamine beta-hydroxylase (DBH) deficiency

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DBH Sequence Analysis

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel

Blueprint Genetics
Finland
6134
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiology Panel

Blueprint Genetics
Finland
12165
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmia Panel

Blueprint Genetics
Finland
760
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DBH

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

devACT® Next Generation Sequencing panel focused on genes that inform actionable clinical management of patients with Developmental Delay, Intellectual Disability, and Autism Spectrum Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
297248
  • L Linkage analysis
  • C Sequence analysis of the entire coding region

Dopamine beta-hydroxylase deficiency (sequence analysis of DBH gene)

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

Test for Dopamine Beta-Hydroxylase Deficiency

Genome Diagnostics Laboratory The Hospital for Sick Children
Canada
11
  • C Sequence analysis of the entire coding region

Results: 1 to 9 of 9

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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