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Results: 41 to 60 of 94

Tests names and labsConditionsGenes, analytes, and microbesMethods

RAF1-Related Disorders via the RAF1 Gene

PreventionGenetics, part of Exact Sciences
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary pediatric cancer panel. NGS panel of 71 genes.

Genologica Medica
Spain
15871
  • C Sequence analysis of the entire coding region

Neurofibromatosis panel. 8-gene NGS panel.

Genologica Medica
Spain
258
  • C Sequence analysis of the entire coding region

Noonan syndrome panel. NGS panel of 22 genes.

Genologica Medica
Spain
4822
  • C Sequence analysis of the entire coding region

RAF1 Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • D Deletion/duplication analysis

Comprehensive Short Stature Genetic Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
8260
  • C Sequence analysis of the entire coding region

Arrhythmia & Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
21193
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
17071
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Hypertrophic

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
8535
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Dilated

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
13448
  • C Sequence analysis of the entire coding region

Noonan Spectrum Disorders Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
3613
  • C Sequence analysis of the entire coding region

RAF1

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

Noonan syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
109
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan and RASopathies NGS Panel

Fulgent Genetics
United States
23526
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defect NGS Panel

Fulgent Genetics
United States
377114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 13 Genes

Reference Laboratory Genetics
Spain
1712
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
4524
  • C Sequence analysis of the entire coding region

Dilated & Arrhythmogenic Cardiomyopathy NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
9251
  • C Sequence analysis of the entire coding region

NOONAN SYNDROME

Laboratorio de Genetica Clinica SL
Spain
811
  • C Sequence analysis of the entire coding region

Results: 41 to 60 of 94

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.