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Results: 1 to 9 of 9

Tests names and labsConditionsGenes and analytesMethods

Invitae Hereditary Prion Disease Test

Invitae
United States
71
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Combined Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel

Invitae
United States
4721
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies Panel Sequencing

ARUP Laboratories, Molecular Genetics and Genomics
United States
3478
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies, PMP22 Deletion/Duplication with Reflex to Sequencing Panel

ARUP Laboratories, Molecular Genetics and Genomics
United States
3478
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dementia all Panel

CeGaT GmbH
Germany
3236
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia (FTD) Panel

CeGaT GmbH
Germany
2928
  • C Sequence analysis of the entire coding region

Choreatic Movement Disorders Panel

CeGaT GmbH
Germany
1621
  • C Sequence analysis of the entire coding region

Genetic Prion Diseases (PRNP)

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

Genetic Prion Diseases

Center for Human Genetics Laboratory University Hospitals - University Hospitals Laboratory Service Foundation
United States
51
  • C Sequence analysis of the entire coding region

Results: 1 to 9 of 9

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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