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Results: 81 to 85 of 85

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CLN8-Related Neuronal Ceroid-Lipofuscinosis

Bioscientia GmbH Center for Human Genetics
Germany
11
  • C Sequence analysis of the entire coding region

CLN8-Related Neuronal Ceroid-Lipofuscinosis

Dep. of Paediatrics and Inherited Metabolic Disorders General University Hospital in Prague and First Faculty of Medicine, Charles University in Prague
Czech Republic
11
  • C Sequence analysis of the entire coding region

Test for CLN8-Related Neuronal Ceroid-Lipofuscinosis

Genome Diagnostics Laboratory Hospital For Sick Children
Canada
11
  • C Sequence analysis of the entire coding region

EPMR, Epilepsy, progressive with mental retardation, CLN8 founder mutation analysis

Laboratory of Genetics HUSLAB
Finland
11
  • T Targeted variant analysis

Results: 81 to 85 of 85

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