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Results: 1 to 11 of 11 (representing 9 labs)

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

Stickler syndrome, autosomal recessive

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

Stickler Syndrome Panel

Blueprint Genetics
Finland
18
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hearing Loss and Deafness Panel

Blueprint Genetics
Finland
8158
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Syndromic Hearing Loss Panel

Blueprint Genetics
Finland
670
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS panel - Stickler syndrome and related disorders

Genome Diagnostics VU University Medical Center
Netherlands
78
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Retina/Photoreceptor Dystrophy: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
36120
  • C Sequence analysis of the entire coding region

Stickler Syndrome Panel

CeGaT GmbH
Germany
65
  • C Sequence analysis of the entire coding region

Stickler Syndrome Panel

CeGaT GmbH
Germany
65
  • C Sequence analysis of the entire coding region

COL2A1 mutational analysis

Connective Tissue Laboratory Ghent University Hospital
Belgium
181
  • E Sequence analysis of select exons

Connective Tissue Disorders Panel

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
4950
  • E Sequence analysis of select exons

Results: 1 to 11 of 11

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