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Results: 81 to 100 of 153

Tests names and labsConditionsGenes, analytes, and microbesMethods

Epilepsy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
13283
  • C Sequence analysis of the entire coding region

Idiopathic and familial epilepsies - different panels

Institute of Human Genetics Cologne University
Germany
15303
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PPM-X Syndrome (MECP2 Single Gene Test)

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Actionable Epilepsy NGS Panel

Fulgent Genetics
United States
7823
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Epilepsy NGS Panel

Fulgent Genetics
United States
509275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MECP2-Related Severe Neonatal Encephalopathy (MECP2 Single Gene Test)

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett Syndrome (MECP2 Single Gene Test)

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing NTNG1

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Rett Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 18 Genes

Reference Laboratory Genetics
Spain
1718
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegia NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
8179
  • C Sequence analysis of the entire coding region

RETT SYNDROME

Laboratorio de Genetica Clinica SL
Spain
33
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett Syndrome, Deletions-Duplications (MLPA) MECP2 Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Rett Syndrome, Sequencing MECP2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Brain malformations

Asper Biogene Asper Biogene LLC
Estonia
318252
  • C Sequence analysis of the entire coding region

Epilepsy Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
143135
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett syndrome

Labor Dr. Wisplinghoff
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PreSeek Non-invasive Prenatal Gene Sequencing Screen

Baylor Genetics
United States
4930
  • C Sequence analysis of the entire coding region

Panel on demand

MGZ Medical Genetics Center
Germany
251
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mental Retardation and Dysmorphology - panels

MGZ Medical Genetics Center
Germany
15343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett - Angelman Syndrome

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
312
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 81 to 100 of 153

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.