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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Prenatal ccfDNA screening for fetal aneuploidy

Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL
Canada
31
  • D Deletion/duplication analysis

Diagnostic génotypique direct au locus HFE (hémochromatose héréditaire)

Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL
Canada
11
  • T Targeted variant analysis

FAH tyrosinemia type I

Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL
Canada
11
  • T Targeted variant analysis

Direct molecular diagnostics of AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN

Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL
Canada
11
  • T Targeted variant analysis

fragile-X syndrome molecular diagnostics

Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL
Canada
11
  • M Methylation analysis
  • T Targeted variant analysis

Diagnostic génotypique direct de la dystrophie myotonique de Steinert (Gène DM)

Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL
Canada
11
  • T Targeted variant analysis

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.