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Results: 61 to 68 of 68

Tests names and labsConditionsGenes, analytes, and microbesMethods

Branchiootorenal syndrome 3

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Branchiootorenal syndrome 1

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Branchiootorenal Spectrum Disorder Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
53
  • C Sequence analysis of the entire coding region

EYA1 sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Hearing Loss-Common and Non-Syndromic Hearing Loss Panel

Genome Diagnostics Laboratory Hospital For Sick Children
Canada
6457
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OtoSeq Hearing Loss Panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
3623
  • C Sequence analysis of the entire coding region

Melnick-Fraser syndrome

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Test for EYA1-Related Branchiootorenal Spectrum Disorders

Genome Diagnostics Laboratory Hospital For Sick Children
Canada
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 61 to 68 of 68

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.