U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 81 to 91 of 91

Tests names and labsConditionsGenes, analytes, and microbesMethods

Parkinson all Panel

CeGaT GmbH
Germany
4248
  • C Sequence analysis of the entire coding region

Epilepsy and X-linked Mental Retardation with Seizures Panel

CeGaT GmbH
Germany
2125
  • C Sequence analysis of the entire coding region

Brain Malformations / Neuronal Migration Disorders

MGZ Medical Genetics Center
Germany
2266
  • C Sequence analysis of the entire coding region

X-Linked Mental Retardation

MGZ Medical Genetics Center
Germany
4113
  • C Sequence analysis of the entire coding region

ATP6AP2 Single Gene

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

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
206118
  • 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

X-linked Non-Specific Intellectual Disability Panel

Genetic Services Laboratory University of Chicago
United States
177
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mental Retardation, X-linked, Syndromic, Hedera type, ATP6AP2

Center for Human Genetics, Inc
United States
11
  • C Sequence analysis of the entire coding region

Results: 81 to 91 of 91

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.