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Results: 1 to 4 of 4

Tests names and labsConditionsGenes, analytes, and microbesMethods

Congenital central hypoventilation syndrome (frequent mutation - PARMs- on PHOX2B gene)

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

Dermatology Panel 

CGC Genetics Unilabs
Portugal
1277
  • C Sequence analysis of the entire coding region

Bone diseases panel_v.2.0

CGC Genetics Unilabs
Portugal
1662
  • C Sequence analysis of the entire coding region

SKELETAL DYSPLASIAS PANEL

Laboratorio de Genetica Clinica SL
Spain
1643
  • E Sequence analysis of select exons

Results: 1 to 4 of 4

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