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Results: 1 to 20 of 146 (representing 57 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Marfan, Loeys-Dietz syndrome and related disorders panel

Centogene AG - the Rare Disease Company
Germany
1715
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive pulmonary disease panel

Centogene AG - the Rare Disease Company
Germany
5766
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Marfan syndrome, type I - Sanger / Del Dup Comprehensive

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Marfan syndrome, type I (MFS1) - Deletion/Duplication

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis

Marfan syndrome, type I (MFS1) - Sanger Sequencing

Connective Tissue Gene Tests
United States
11
  • C Sequence analysis of the entire coding region

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

PulmoGene Panel (64 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
6964
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Marfan Syndrome, Type 2 - TGFBR1 Gene

Center for Genetics at Saint Francis Saint Francis Hospital
United States
51
  • C Sequence analysis of the entire coding region

Marfan Syndrome, Type 2 - TGFBR2 Gene

Center for Genetics at Saint Francis Saint Francis Hospital
United States
51
  • C Sequence analysis of the entire coding region

Marfan Syndrome - FBN1 Gene

Center for Genetics at Saint Francis Saint Francis Hospital
United States
31
  • C Sequence analysis of the entire coding region

Marfan Syndrome, FBN1 Seq, Del/Dup

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Marfan Syndrome (FBN1) Sequencing

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
81
  • C Sequence analysis of the entire coding region

Sudden Cardiac Arrest Sequencing Panel

PreventionGenetics
United States
6349
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiology Sequencing Panel

PreventionGenetics
United States
190164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial Thoracic Aortic Aneurysm and Dissection (TAAD) Sequencing Panel

PreventionGenetics
United States
1212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Aortic diseases Panel

Health in Code S.L.
Spain
7135
  • C Sequence analysis of the entire coding region

Aortic Valvular Diseases Panel

Health in Code S.L.
Spain
6030
  • C Sequence analysis of the entire coding region

Marfan-Syndrome

Human Genetics University Hospital Bern
Switzerland
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 146

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.

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