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Results: 1 to 20 of 23 (representing 18 labs)

Tests names and labsConditionsGenes and analytesMethods

Distal Arthrogryposis Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
1110
  • C Sequence analysis of the entire coding region

Distal Arthrogryposis Deletion/Duplication Analysis

Genetic Services Laboratory University of Chicago
United States
1110
  • D Deletion/duplication analysis

Arthrogryposis, distal type 2A

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Neuromuscular Sequencing Panel

PreventionGenetics
United States
148124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Distal Arthrogryposis Sequencing Panel

PreventionGenetics
United States
1311
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MYH3. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

MYH3 -Related Distal Arthrogryposis via the MYH3 Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

ARTHROGRYPOSIS, DISTAL, TYPE 2A (FREEMAN-SHELDON SYNDROME)

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Distal Arthrogryposis Type 2A , Sequencing MYH3 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Neuromuscular Comprehensive Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
454305
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ARTHROGRYPOSIS

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
47
  • C Sequence analysis of the entire coding region

Distal arthrogryposis type 2A

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

Freeman Sheldon Syndrome

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

Single gene testing MYH3

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Freeman-Sheldon syndrome (sequence analysis of MYH3 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

MYH3

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Distal Arthrogryposis Syndromes NGS Panel

Fulgent Genetics
United States
54
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arthrogryposis, distal 2A

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

Arthrogryposis, distal 2A

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

Arthrogryposis type 2, Distal: MYH3 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
21
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 23

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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