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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

LDHB - NGS including CNV analysis

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

[Lactate dehydrogenase-B deficiency], 614128; LDHBD (Glycogen storage disease due to lactate dehydrogenase deficiency) (LDHB 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

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Pyruvate Metabolism Disorders NGS Panel

Fulgent Genetics
United States
1814
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LDHB 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
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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