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Results: 41 to 55 of 55

Tests names and labsConditionsGenes, analytes, and microbesMethods

HSP, Complete Dominant Evaluation

Athena Diagnostics
United States
1710
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HSP, Supplemental Sporadic Evaluation

Athena Diagnostics
United States
2422
  • C Sequence analysis of the entire coding region

HSP, Comprehensive Evaluation

Athena Diagnostics
United States
4024
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HSP, Common Dominant Evaluation

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

Hereditary spastic paraplegia (HSP), autosomal dominant and X-linked Panel

CeGaT GmbH
Germany
2217
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegia

Asper Biogene Asper Biogene LLC
Estonia
3938
  • C Sequence analysis of the entire coding region

Autosomal dominant spastic paraplegia type 10

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

Single gene testing KIF5A

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
146143
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Disease

Asper Biogene Asper Biogene LLC
Estonia
8974
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KIF5A Single Gene

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

Charcot Marie Tooth Disease Extended NGS Panel

Fulgent Genetics
United States
17259
  • 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

Spastic Paraplegia NGS Panel

Fulgent Genetics
United States
5327
  • 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

Results: 41 to 55 of 55

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.