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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

VANGL1 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Caudal regression syndrome, 600145, Autosomal dominant (Sirenomelia) (VANGL1 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

Caudal regression syndrome, 600145, Autosomal dominant (Sirenomelia) (VANGL1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

SACRAL DEFECT WITH ANTERIOR MENINGOCELE (Sirenomelia) (VANGL1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Caudal regression syndrome

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

VANGL1 Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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