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Results: 21 to 31 of 31

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hyperammonemia and Urea Cycle Disorder NGS Panel

Fulgent Genetics
United States
7056
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Homocystinuria Core Panel

Blueprint Genetics
Finland
14
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Organic Acidemia/Aciduria & Cobalamin Deficiency Panel

Blueprint Genetics
Finland
653
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HCFC1 Single Gene

Fulgent Genetics
United States
131
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS panel - Ectopia lentis and/or Weill-Marchesani syndrome

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
57
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Marfan/TAAD Sequencing Panel

GeneDx
United States
916
  • S Mutation scanning of the entire coding region

Clinical Exome

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

XLID (X-Linked Intellectual Disability) NGS Panel

Fulgent Genetics
United States
162117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amino Acid Analysis, Plasma

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
1917
  • A Analyte

Results: 21 to 31 of 31

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