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Results: 21 to 40 of 82

Tests names and labsConditionsGenes, analytes, and microbesMethods

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • C Sequence analysis of the entire coding region

Invitae Metabolic Newborn Screening Confirmation Panel

Invitae
United States
201158
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Fatty Acid Oxidation Defects Panel

Invitae
United States
2825
  • D Deletion/duplication analysis

Fatty Acid Oxidation Panel (MitomeNGS)

Baylor Genetics
United States
1617
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

ACADS Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
11
  • T Targeted variant analysis

ACADS Sequence Analysis

Baylor Genetics
United States
11
  • C Sequence analysis of the entire coding region

ACADS Deletion/Duplication Analysis

Baylor Genetics
United States
11
  • D Deletion/duplication analysis

ACADS Comprehensive - Sequence & Deletion/Duplication Analysis

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

Short Chain Acyl-CoA Dehydrogenase Deficiency via the ACADS Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Acylcarnitine Analysis - Plasma

Baylor Genetics
United States
2327
  • A Analyte

Comprehensive Epilepsy

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
414800
  • C Sequence analysis of the entire coding region

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Hyperammonemia and urea cycle disorders panel. 48-gene NGS panel.

Genologica Medica
Spain
4948
  • C Sequence analysis of the entire coding region

Fatty acid oxidation syndrome panel. NGS panel of 26 genes.

Genologica Medica
Spain
3026
  • C Sequence analysis of the entire coding region

General panel of metabolic myopathies

Genologica Medica
Spain
114110
  • C Sequence analysis of the entire coding region

Acyl-CoA dehydrogenase, short-chain, deficiency of: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Fatty Acid Oxidation Disorders Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
2325
  • C Sequence analysis of the entire coding region

Fatty Acid Oxidation Disorders Gene Panel

Duzen Laboratories Duzen BBAGUAS
Turkey
119
  • C Sequence analysis of the entire coding region

Acyl-CoA dehydrogenase, short-chain, deficiency of

Bioarray
Spain
11
  • D Deletion/duplication analysis

Results: 21 to 40 of 82

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.