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Results: 81 to 88 of 88

Tests names and labsConditionsGenes, analytes, and microbesMethods

Paraganglioma-pheochromocytoma 3 (PGL3) syndrome , Hereditary -SDHC gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Paraganglioma-pheochromocytoma syndrome , Hereditary: SDHB, SDHC and SDHD genes sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
33
  • C Sequence analysis of the entire coding region

SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

MGZ Medical Genetics Center
Germany
11
  • C Sequence analysis of the entire coding region

Hereditary Paraganglioma

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
11
  • C Sequence analysis of the entire coding region

Hereditary Phaeochromocytoma/Paraganglioma Syndromes (MAX, SDHAF2, SDHB, SDHC, SDHD, TMEM127, VHL)

Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital
New Zealand
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paragangliomas 3

Center for Human Genetics, Inc
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

Cancer Genomic Medicine Translational Research Lab Cleveland Clinic Genomic Medicine Institute
United States
11
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Hereditary Paraganglioma-Pheochromocytoma Syndrome

Cancer Genomic Medicine Translational Research Lab Cleveland Clinic Genomic Medicine Institute
United States
43
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Results: 81 to 88 of 88

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