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Results: 1 to 20 of 27

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
6021038
  • C Sequence analysis of the entire coding region

Mental retardation, X-linked, associated with fragile site FRAXE

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

X-Linked Intellectual Disability NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
8081
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
242171
  • D Deletion/duplication analysis

Mental retardation, X-linked, non-syndromic

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3531
  • C Sequence analysis of the entire coding region

Mental retardation, X-linked (NGS panel for 89 genes)

CGC Genetics
Portugal
4989
  • C Sequence analysis of the entire coding region

X-linked mental retardation (deletion/duplication analysis, multiple genes)

CGC Genetics
Portugal
1516
  • D Deletion/duplication analysis

Mental retardation, X-linked, FRAXE type (AFF2 gene, msTP-PCR)

CGC Genetics
Portugal
11
  • M Methylation analysis

X-Linked Intellectual Disability Panel, Sequencing, 76 Genes

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
12776
  • C Sequence analysis of the entire coding region

AFF2

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

devSEEKĀ® Sequence Analysis for Neurodevelopmental Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
261201
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism Panel: Tier 2

Emory Genetics Laboratory Emory University
United States
10360
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

X-linked Intellectual Disability: Gene Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
13991
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

XLID NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
188107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
752392
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fragile X syndrome E

MedGene
Slovakia
11
  • M Methylation analysis

Fragile X syndrome E

Praxis fuer Humangenetik Wien
Austria
11
  • M Methylation analysis

Fragile X syndrome type E: FMR2 gene CCG Expansion

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • T Targeted variant analysis

FRAXE Syndrome MALE (Rpts & Methylation)

Emory Genetics Laboratory Emory University
United States
11
  • M Methylation analysis
  • T Targeted variant analysis

FRAXE Syndrome FEMALE (Rpts Only)

Emory Genetics Laboratory Emory University
United States
11
  • T Targeted variant analysis

Results: 1 to 20 of 27

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.