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Results: 141 to 160 of 170

Tests names and labsConditionsGenes, analytes, and microbesMethods

Noonan Syndrome and related disorders (RASopathies) Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
3111
  • 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

Non-Immune Hydrops NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
8687
  • 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

Heterotaxy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
156114
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
12583
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Costello syndrome (HRAS)

MVZ Dr. Eberhard & Partner Dortmund
Germany
21
  • C Sequence analysis of the entire coding region

Costello syndrome (HRAS)

MVZ Dr. Eberhard & Partner Dortmund
Germany
21
  • C Sequence analysis of the entire coding region

Costello syndrome (HRAS)

MVZ Dr. Eberhard & Partner Dortmund
Germany
21
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

HRAS Single Gene

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy NGS Panel

Fulgent Genetics
United States
37586
  • 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

Noonan Spectrum Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
4231
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lysosomal Disorders NGS Panel

Fulgent Genetics
United States
186106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital heart defects panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
6934
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Costello syndrome

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Congenital myopathy with excess of muscle spindles

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Results: 141 to 160 of 170

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.