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Results: 1 to 4 of 4

Tests names and labsConditionsGenes, analytes, and microbesMethods

ARNT2 - NGS including CNV analysis

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

Webb-Dattani syndrome, 615926, Autosomal recessive; WEDAS (Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome) (ARNT2 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

Webb-Dattani syndrome, 615926, Autosomal recessive; WEDAS (Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome) (ARNT2 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

Webb-Dattani syndrome: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Results: 1 to 4 of 4

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