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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

GUCY1A1 - NGS including CNV analysis

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

Blood Coagulation Panel

Centogene AG - the Rare Disease Company
Germany
110112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel

PreventionGenetics, part of Exact Sciences
United States
346160
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Hereditary Moyamoya Disease Panel 

Labcorp Genetics (formerly Invitae) LabCorp
United States
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Moyamoya 6 with achalasia, 615750, Autosomal recessive (Moyamoya disease with early-onset achalasia) (GUCY1A3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Moyamoya disease: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
33
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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