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Results: 81 to 91 of 91

Tests names and labsConditionsGenes, analytes, and microbesMethods

HAD panel 1

Connective Tissue Laboratory Ghent University Hospital
Belgium
1510
  • C Sequence analysis of the entire coding region

TGFB3 mutational analysis

Connective Tissue Laboratory Ghent University Hospital
Belgium
151
  • E Sequence analysis of select exons

TGFBR1 mutational analysis

Connective Tissue Laboratory Ghent University Hospital
Belgium
151
  • E Sequence analysis of select exons

TGFB2 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

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

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

Results: 81 to 91 of 91

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.