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Results: 41 to 60 of 72

Tests names and labsConditionsGenes, analytes, and microbesMethods

Noonan Syndrome Panel by NGS

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
12
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

NOONAN SYNDROME

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

Rasopathy NextGen Panel

Children's Hospital Colorado Precision Diagnostics Laboratory Children's Hospital Colorado
United States
1220
  • C Sequence analysis of the entire coding region

Noonan Spectrum Disorders Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
2421
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel

Blueprint Genetics
Finland
6155
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiology Panel

Blueprint Genetics
Finland
12185
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Syndrome Panel

Blueprint Genetics
Finland
422
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Syndrome Panel

Genetic Services Laboratory University of Chicago
United States
117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RIT1 Single Gene

Fulgent Genetics
United States
651
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RPL6 Single Gene

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

NRAS Single Gene

Fulgent Genetics
United States
1781
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
128130
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Syndrome 11-Gene Sequencing Panel

Center for Human Genetics, Inc
United States
111
  • C Sequence analysis of the entire coding region

Invitae Congenital Heart Defects and Heterotaxy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
12882
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Syndrome Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RASopathy NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
723
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

Noonan syndrome, PTPN11 sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • C Sequence analysis of the entire coding region

Results: 41 to 60 of 72

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.