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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Amelogenesis imperfecta, type IIA3, 613211, Autosomal recessive; AI2A3 (Amelogenesis imperfecta) (WDR72 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 WDR72 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

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

Amelogenesis Imperfecta and Dentinogenesis Imperfecta Panel

Blueprint Genetics
Finland
915
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amelogenesis Imperfecta , Panel Massive Sequencing (NGS) 9 Genes

Reference Laboratory Genetics
Spain
109
  • 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

WDR72 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
51294672
  • 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, Hypomaturation Type, IIA3

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

Results: 1 to 13 of 13

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.