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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Riboflavin deficiency, 615026, Autosomal dominant; RBFVD (Maternal riboflavin deficiency) (SLC52A1 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

Riboflavin deficiency, 615026, Autosomal dominant; RBFVD (Maternal riboflavin deficiency) (SLC52A1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Disorders of Fatty Acid Oxidation (FAOD) Panel

PreventionGenetics, part of Exact Sciences
United States
3232
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Motor Neuron Disorder and Related Diseases , Panel Massive Sequencing (NGS) 49 Genes

Reference Laboratory Genetics
Spain
6049
  • C Sequence analysis of the entire coding region

SLC52A1 Single Gene

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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