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Results: 1 to 10 of 10

Tests names and labsConditionsGenes, analytes, and microbesMethods

Pachyonychia congenita 2, 167210, Autosomal dominant; PC2 (Pachyonychia congenita) (KRT17 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

Congenital pachyonychia panel. 7-gene NGS panel.

Genologica Medica
Spain
107
  • C Sequence analysis of the entire coding region

Palmoplantar keratoderma panel. 25-gene NGS panel.

Genologica Medica
Spain
6225
  • C Sequence analysis of the entire coding region

KRT17

Institute for Human Genetics University Medical Center Freiburg
Germany
21
  • C Sequence analysis of the entire coding region

Steatocystoma Multiplex (KRT17 Single Gene Test)

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pachyonychia Congenita NGS Panel

Fulgent Genetics
United States
228
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pachyonychia congenita type 2

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Ichthyoses and related disorders of cornification Panel

CeGaT GmbH
Germany
4265
  • C Sequence analysis of the entire coding region

KRT17 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 10 of 10

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