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Results: 41 to 47 of 47

Tests names and labsConditionsGenes, analytes, and microbesMethods

GJB2

Institute of Human Genetics Medical University Innsbruck
Austria
71
  • S Mutation scanning of the entire coding region

GJB2 Single Gene

Fulgent Genetics
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GJB2/GJB6-Related DFNA3 Nonsyndromic Hearing Loss and Deafness (GJB2/GJB6)

MVZ Dr. Eberhard & Partner Dortmund
Germany
52
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Keratitis-Ichthyosis-Deafness, Autosomal Dominant

Molecular Diagnostics Lab Nemours Children's Health, Delaware
United States
11
  • C Sequence analysis of the entire coding region

GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2/GJB6)

MVZ Dr. Eberhard & Partner Dortmund
Germany
52
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 47 of 47

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