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Results: 141 to 155 of 155

Tests names and labsConditionsGenes, analytes, and microbesMethods

X-Linked Intellectual Disability (XLID) NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1114
  • C Sequence analysis of the entire coding region

Syndromic Autism NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
183
  • 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

Coffin-Siris and Nicolaides-Baraitser Syndrome (CSS, NCBRS)

MGZ Medical Genetics Center
Germany
27
  • 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

PHF6 Single Gene

Fulgent Genetics
United States
11
  • 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

XLID (X-Linked Intellectual Disability) NGS Panel

Fulgent Genetics
United States
162117
  • 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

Autism NGS Panel

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

Bardet Biedl Syndrome

Asper Biogene Asper Biogene LLC
Estonia
2425
  • C Sequence analysis of the entire coding region

Coffin-Siris syndrome

Institute of Human Genetics Cologne University
Germany
97
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Borjeson-Forssman-Lehmann syndrome

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

Results: 141 to 155 of 155

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.