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Results: 1 to 11 of 11

Tests names and labsConditionsGenes and analytesMethods

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
124129
  • E Sequence analysis of select exons

Deafness, autosomal dominant type 48

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

Non syndromic deafness AD, AR and XL (NGS panel for 79 genes)

CGC Genetics
Portugal
7479
  • C Sequence analysis of the entire coding region

Syndromic and non syndromic deafness (NGS panel for 127 genes)

CGC Genetics
Portugal
118127
  • C Sequence analysis of the entire coding region

Non syndromic deafness AD (NGS panel for 33 genes)

CGC Genetics
Portugal
3032
  • C Sequence analysis of the entire coding region

Deafness, autosomal dominant 48 (sequence analysis of MYO1A gene)

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

MYO1A

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

Sensorineural Hearing Loss

Asper Biogene Asper Biogene LLC
Estonia
8177
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hearing Loss: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
15992
  • C Sequence analysis of the entire coding region

Hearing Loss NGS Panel

Fulgent Genetics
United States
202103
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DFNA48 Nonsyndromic Hearing Loss and Deafness

Bioscientia GmbH Center for Human Genetics
Germany
11
  • C Sequence analysis of the entire coding region

Results: 1 to 11 of 11

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