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Results: 1 to 8 of 8

Tests names and labsConditionsGenes, analytes, and microbesMethods

Lipid Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
8071
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hypertriglyceridemia NGS Panel

Fulgent Genetics
United States
2015
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neutral Lipid Storage Disease With Myopathy (PNPLA2 Single Gene Test)

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

PNPLA2 Single Gene

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

Limb-Girdle Muscular Dystrophy NGS Panel

Fulgent Genetics
United States
5120
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51304674
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular NGS Panel

Fulgent Genetics
United States
280112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophies NGS Panel

Fulgent Genetics
United States
12542
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 8 of 8

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