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Results: 1 to 13 of 13

Tests names and labsConditionsGenes and analytesMethods

Hypermanganesemia with dystonia, polycythemia, and cirrhosis

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

Comprehensive Neurogenetics Panel (359 genes)

Sherbrooke Genomic Medicine
Canada
6035
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

Single gene testing SLC30A10

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

Dystonia All Panel

CeGaT GmbH
Germany
4953
  • C Sequence analysis of the entire coding region

Dystonia Plus Syndrome Panel

CeGaT GmbH
Germany
1514
  • C Sequence analysis of the entire coding region

Parkinson Syndrome, autosomal recessive Panel

CeGaT GmbH
Germany
911
  • C Sequence analysis of the entire coding region

Parkinson Dystonia Panel

CeGaT GmbH
Germany
59
  • C Sequence analysis of the entire coding region

Atypical Parkinson syndrome Panel

CeGaT GmbH
Germany
2524
  • C Sequence analysis of the entire coding region

Parkinson all Panel

CeGaT GmbH
Germany
4248
  • C Sequence analysis of the entire coding region

Parkinson Syndrome, autosomal dominant Panel

CeGaT GmbH
Germany
910
  • C Sequence analysis of the entire coding region

Hypermanganesemia with dystonia, polycythemia and cirrhosis (sequence analysis of SLC30A10 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

SLC30A10

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

Results: 1 to 13 of 13

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