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Results: 81 to 93 of 93

Tests names and labsConditionsGenes, analytes, and microbesMethods

Multiple cutaneous and uterine leiomyomas

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

FH 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

TCA Cycle NGS Panel

Fulgent Genetics
United States
1515
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lysosomal Disorders NGS Panel

Fulgent Genetics
United States
186106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lactic Acidosis-Pyruvate NGS Panel

Fulgent Genetics
United States
9569
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Multiple cutaneous and uterine leiomyomata

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Fumarase deficiency

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Organic Acids, Comprehensive, Quantitative, Urine

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
3857
  • A Analyte

Multiple cutaneous and uterine leiomyomata

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Fumarase deficiency

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Fumarase deficiency

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 81 to 93 of 93

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.