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Results: 1 to 4 of 4

Tests names and labsConditionsGenes, analytes, and microbesMethods

Ectodermal dysplasia 13, hair/tooth type, 617392, Autosomal recessive; ECTD13 (KREMEN1 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

Ectodermal dysplasia 13, hair/tooth type, 617392, Autosomal recessive; ECTD13 (KREMEN1 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

Invitae Ectodermal Dysplasia and Related Disorders Panel

Invitae
United States
14873
  • D Deletion/duplication analysis

Ectodermal dysplasia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1311
  • C Sequence analysis of the entire coding region

Results: 1 to 4 of 4

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