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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

Neural tube defects, 182940, Autosomal dominant (Neural tube closure defect) (VANGL2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Neural tube defect (sequence analysis of VANGL2 gene)

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

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Neural Tube Defects and Related Disorders , Panel Massive Sequencing (NGS) 9 Genes

Reference Laboratory Genetics
Spain
39
  • C Sequence analysis of the entire coding region

VANGL2, full sequencing

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

VANGL2 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

Spina bifida

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Spina bifida

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Results: 1 to 9 of 9

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