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Results: 21 to 40 of 41

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hypothyroidism and thyroid hormone resistance panel. NGS panel of 21 genes.

Genologica Medica
Spain
4221
  • C Sequence analysis of the entire coding region

Interstitial lung disease panel. 25-gene NGS panel.

Genologica Medica
Spain
4025
  • C Sequence analysis of the entire coding region

Complete panel of pulmonology. NGS panel of 66 genes.

Genologica Medica
Spain
11466
  • C Sequence analysis of the entire coding region

Lung Surfactant Deficiency. Panel NGS genes: ABCA3, FOXF1, NKX2-1, SFTPB, SFTPC.

Genologica Medica
Spain
75
  • C Sequence analysis of the entire coding region

Choreoathetosis, hypothyroidism, and neonatal respiratory distress: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Comprehensive lung panel

Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
6466
  • C Sequence analysis of the entire coding region

Brain-Lung-Thyroid Syndrome (NKX2-1 Single Gene Test)

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

Hypothyroidism and Resistance to Thyroid Hormone NGS Panel

Fulgent Genetics
United States
4119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NKX2-1 Related Disorders: gene sequencing

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

Surfactant Dysfunction & Respiratory Distress in Premature Infants NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1211
  • C Sequence analysis of the entire coding region

Hermansky-Pudlak Syndrome & Pulmonary Fibrosis NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3640
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
123124
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary-Vascular Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
10086
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Respiratory Distress Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
3226
  • 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
51244672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 41

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.