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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

FSHD (Facioscapulohumeral muscular dystrophy) TYPE 1

Revvity Omics Revvity
United States
11
  • X Mutation scanning of select exons

Facioscapulohumeral muscular dystrophy type 1 (FSHD1)

Molecular Diagnostics Platform_Biogipuzkoa Health Research Institute Biogipuzkoa Health Research Institute
Spain
11
  • D Deletion/duplication analysis

SMCHD1 Single Gene

Fulgent Genetics
United States
151
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophies Panel

CeGaT GmbH
Germany
3732
  • C Sequence analysis of the entire coding region

FRG1 Single Gene

Fulgent Genetics
United States
11
  • 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

Facioscapulohumeral muscular dystrophy 1A

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis

Results: 1 to 7 of 7

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