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Results: 41 to 53 of 53

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hearing Loss NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
198157
  • C Sequence analysis of the entire coding region

Waardenburg disease type 1

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Waardenburg Syndrome

Asper Biogene Asper Biogene LLC
Estonia
97
  • C Sequence analysis of the entire coding region

Genetic disorders with abnormal pigmentation Panel

CeGaT GmbH
Germany
2932
  • C Sequence analysis of the entire coding region

Hermansky-Pudlak Syndrome/Oculocutaneous Albinism/Pigmentation panel

Molecular Vision Laboratory
United States
4529
  • C Sequence analysis of the entire coding region

PAX3 Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Waardenburg 1

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Waardenburg Syndrome NGS Panel

Fulgent Genetics
United States
196
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Albinism NGS Panel

Fulgent Genetics
United States
5228
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Waardenburg 1

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

Waardenburg Syndrome

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • L Linkage analysis
  • C Sequence analysis of the entire coding region

Waardenburg Syndrome Type 1/Type 3

Center for Human Genetics, Inc
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 53 of 53

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.