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Results: 21 to 29 of 29

Tests names and labsConditionsGenes, analytes, and microbesMethods

NKX2-1 Related Disorders: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
21
  • C Sequence analysis of the entire coding region

CHOREA, HEREDITARY BENIGN

Laboratorio de Genetica Clinica SL
Spain
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NKX2-1 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Single gene testing NKX2-1

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Choreatic Movement Disorders Panel

CeGaT GmbH
Germany
1621
  • C Sequence analysis of the entire coding region

NKX2-1 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Surfactant NGS Panel

Fulgent Genetics
United States
75
  • 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

Benign hereditary chorea

Molecular Diagnostics Lab Nemours Children's Health, Delaware
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 29 of 29

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.