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Results: 1 to 2 of 2

Tests names and labsConditionsGenes, analytes, and microbesMethods

Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency , Familial hyperaldosteronism type 1 , Familial hypoaldosteronism , 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency (deletions/duplications in the CYP

CGC Genetics Unilabs
Portugal
13
  • D Deletion/duplication analysis

CLVS1 Single Gene

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

Results: 1 to 2 of 2

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