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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Infantile-onset multisystem neurologic, endocrine, and pancreatic disease, 616263, Autosomal recessive (Infantile multisystem neurologic-endocrine-pancreatic disease) (PTRH2 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

Infantile-onset multisystem neurologic, endocrine, and pancreatic disease, 616263, Autosomal recessive (Infantile multisystem neurologic-endocrine-pancreatic disease) (PTRH2 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

PTRH2 - Infantile-onset multisystem neurologic, endocrine, and pancreatic disease

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

Ataxia Exome

Genetic Services Laboratory University of Chicago
United States
289481
  • C Sequence analysis of the entire coding region

PTRH2 Single Gene

Fulgent Genetics
United States
241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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