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Results: 181 to 197 of 197

Tests names and labsConditionsGenes, analytes, and microbesMethods

Teenager Stroke / Stroke-Like Episodes

MGZ Medical Genetics Center
Germany
221
  • C Sequence analysis of the entire coding region

Thoracic Aortic Aneurysms and Aortic Dissections (TAAD)

MGZ Medical Genetics Center
Germany
316
  • C Sequence analysis of the entire coding region

Cobalamin/Propionate/Homocysteine Metabolism Related Disorders Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
2629
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CBS 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

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiovascular disorders panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2917
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Connective Tissue NGS Panel

Fulgent Genetics
United States
18760
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cobalamin Homocysteine Methionine NGS Panel

Fulgent Genetics
United States
2320
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (CBS)

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Marfan Syndrome and Thoracic Aortic Aneurysm and Dissection NGS Panel

Fulgent Genetics
United States
6531
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Thoracic Aortic Aneurysm Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
6249
  • C Sequence analysis of the entire coding region

Aortopathy Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
2728
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency

Dep. of Paediatrics and Inherited Metabolic Disorders General University Hospital in Prague and First Faculty of Medicine, Charles University in Prague
Czech Republic
11
  • A Analyte
  • E Enzyme assay
  • C Sequence analysis of the entire coding region

Hyperhomocysteïnemia due to cysthationine beta-synthase (CBS) deficiency

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • A Analyte
  • C Sequence analysis of the entire coding region

Results: 181 to 197 of 197

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.