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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Amelogenesis imperfecta, type III, 130900, Autosomal dominant (Amelogenesis imperfecta) (FAM83H 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

Amelogenesis and Dentinogenesis Imperfecta Panel

PreventionGenetics, part of Exact Sciences
United States
2834
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amelogenesis Imperfecta via the FAM83H Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiomyopathy Panel (37 genes)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
437
  • X Mutation scanning of select exons
  • S Mutation scanning of the entire coding region

Amelogenesis imperfecta type III (sequence analysis of FAM83H gene)

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

Amelogenesis imperfecta and dentinogenesis imperfecta panel. NGS panel of 15 genes.

Genologica Medica
Spain
2214
  • C Sequence analysis of the entire coding region

Amelogenesis imperfecta: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1817
  • C Sequence analysis of the entire coding region

qGenEx Craniofacial Anomalies

Quantitative Genomic Medicine Laboratories, SL
Spain
135136
  • C Sequence analysis of the entire coding region

FAM83H Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amelogenesis imperfecta panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
108
  • C Sequence analysis of the entire coding region

Amelogenesis Imperfecta NGS Panel

Fulgent Genetics
United States
7531
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amelogenesis Imperfecta, Type IIIA

Dental Research Laboratory University of Michigan School of Dentistry
United States
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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