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Results: 1 to 6 of 6 (representing 5 labs)

Tests names and labsConditionsGenes and analytesMethods

Primary Immunodeficiency Panel

Blueprint Genetics
Finland
2232
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Complement System Disorder Panel

Blueprint Genetics
Finland
182
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CLU

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

Alzheimer: MAPT, CLU, PICALM, CR1 genes screening

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
44
  • X Mutation scanning of select exons

Atypical Hemolytic-Uremic Syndrome Panel

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

AHUS/MPGN panel

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
213
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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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