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Results: 1 to 20 of 30 (representing 13 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Comprehensive pulmonary disease panel

Centogene AG - the Rare Disease Company
Germany
5766
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Surfactant metabolism dysfunction

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Surfactant metabolism dysfunction type 4

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pulmonary Fibrosis - Hermansky Pudlak Panel (21 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
2321
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PulmoGene Panel (64 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
6964
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Basic Fibrosis Panel (12 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
1212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CSF2RA. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
242171
  • D Deletion/duplication analysis

Surfactant Dysfunction and Respiratory Distress in Premature Infants Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
88
  • C Sequence analysis of the entire coding region

Hermansky-Pudlak and Pulmonary Fibrosis Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
2325
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
9293
  • C Sequence analysis of the entire coding region

Pulmonary Surfactant Metabolism Dysfunction Type 4, Sequencing CSF2RA Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary-Vascular Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
5964
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary-Vascular Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
5964
  • D Deletion/duplication analysis

Comprehensive Pulmonary-Vascular Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
6065
  • C Sequence analysis of the entire coding region

Neonatal Respiratory Distress Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1616
  • C Sequence analysis of the entire coding region

Neonatal Respiratory Distress Seq + Del/ Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1616
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Respiratory Distress Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1616
  • D Deletion/duplication analysis

Results: 1 to 20 of 30

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.

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