Filters

See more specimen types...

Other countries

Results: 1 to 15 of 15 (representing 10 labs)

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

Mental retardation, X-linked type 46

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

X-chromosome High Resolution microarray analysis

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

ARHGEF6-Related X-Linked Intellectual Disability (XLID)

Ambry Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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 type 46 (sequence analysis of ARHGEF6 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

ARHGEF6

Fulgent Genetics
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

XLID NGS Panel

Fulgent Genetics
United States
187107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

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

XLMR 46: ARHGEF6 Gene Deletion/Duplication

Emory Genetics Laboratory Emory University
United States
11
  • D Deletion/duplication analysis

XLMR 46: ARHGEF6 Full Gene Sequencing

Emory Genetics Laboratory Emory University
United States
11
  • C Sequence analysis of the entire coding region

X-linked mental retardation 46

Center for Human Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 15 of 15

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.

Support Center