Filters

See more specimen types...

Other countries

Results: 1 to 8 of 8

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

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

VANGL1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Caudal Regression Syndrome , Sequencing VANGL1 Gene

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

Caudal regression syndrome

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Caudal regression syndrome (sequence analysis of VANGL1 gene)

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

VANGL1

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

Epilepsy NGS Panel

Fulgent Genetics
United States
597343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Caudal Dysgenesis Syndrome

Keegan Laboratory University of Michigan
United States
11
  • X Mutation scanning of select exons

Results: 1 to 8 of 8

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