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Results: 121 to 140 of 146

Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

XLID (X-Linked Intellectual Disability) NGS Panel

Fulgent Genetics
United States
162117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett-Angelman NGS Panel

Fulgent Genetics
United States
7730
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Migraine NGS Panel

Fulgent Genetics
United States
4419
  • D Deletion/duplication analysis
  • 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

Epileptic syndromes with epilepsy and intellectual disability panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
7450
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Epileptic encephalopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
5332
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Genetics
United States
170106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Rett syndrome

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MECP2-Related Disorders

MGZ Medical Genetics Center
Germany
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MECP2 Del/Dup

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
11
  • D Deletion/duplication analysis

MECP2 Seq

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
11
  • C Sequence analysis of the entire coding region

MECP2 Seq + Del/Dup

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MECP2 mutation analysis

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MECP2-Related Disorders

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett Syndrome

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett Syndrome

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
12
  • C Sequence analysis of the entire coding region

Results: 121 to 140 of 146

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.