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Results: 1 to 8 of 8 (representing 7 labs)

Tests names and labsConditionsGenes and analytesMethods

Glycogen storage disease type IC

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

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
329300
  • C Sequence analysis of the entire coding region

Severe Congenital Neutropenia Gene Set

Genomics and Pathology Services Washington University in St.Louis
United States
1524
  • C Sequence analysis of the entire coding region

Glycogen storage disease type 1

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Metabolic Myopathies Panel

CeGaT GmbH
Germany
2641
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Syndromes Deletion/Duplication Panel

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
4355
  • D Deletion/duplication analysis

Glycogen storage disease due to glucose-6-phosphatase deficiency type 1B (sequence analysis of SLC37A4 gene)

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

Bone Marrow Failure Syndromes Panel by next-generation sequencing (NGS)

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
4759
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 8 of 8

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