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Results: 1 to 2 of 2

Tests names and labsConditionsGenes, analytes, and microbesMethods

Okur-Chung neurodevelopmental syndrome, 617062, Autosomal dominant (CSNK2A1 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

Okur-Chung neurodevelopmental syndrome, 617062, Autosomal dominant (CSNK2A1 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

Results: 1 to 2 of 2

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