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Results: 1 to 5 of 5

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cerebrooculofacioskeletal syndrome 4 (sequence analysis of ERCC1 gene)

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

Pseudohypoparathyroidism, type IB, 603233, Autosomal dominant (Pseudohypoparathyroidism type 1B) (GNAS-AS1 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

Genomic Unity® Renal Disorders Analysis

Variantyx, Inc.
United States
1425
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • 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

Pseudohypoparathyroidism, type IB

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
13
  • D Deletion/duplication analysis
  • M Methylation analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 5 of 5

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