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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K, 607831, Autosomal recessive, Autosomal dominant; CMT2K (Autosomal recessive Charcot-Marie-Tooth disease with hoarseness) (JPH1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Neuropathy Panel

Mendelics
Brazil
1104
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Xpanded Adult Movement Disorders Panel

GeneDx
United States
5473
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth disease: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
6854
  • C Sequence analysis of the entire coding region

JPH1 Single Gene

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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