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Results: 1 to 4 of 4

Tests names and labsConditionsGenes, analytes, and microbesMethods

Deafness autosomal dominant 13 , Deafness autosomal recessive 53 , Fibrochondrogenesis 2 , Stickler type 3 syndrome , Weissenbacher-Zweymuller syndrome (sequence analysis of COL11A2 gene)

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

PHB2 - Prohibitin deficiency

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

MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES)

Laboratorio de Genetica Clinica SL
Spain
11372
  • E Sequence analysis of select exons

PHB2 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 4 of 4

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