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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hypotrichosis 12, 615885, Autosomal dominant; HYPT12 (Hypotrichosis simplex) (RPL21 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

RPL21 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoSkin Panel

Centogene AG - the Rare Disease Company
Germany
157151
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypotrichosis NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
1010
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypotrichosis Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
1010
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypotrichosis Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
1010
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypotrichosis Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
1010
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypotrichosis NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
1010
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypotrichosis Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
1010
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Ectodermal Dysplasia and Related Disorders Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
14873
  • D Deletion/duplication analysis

Hypotrichosis: Full gene sequencing panel

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

Nonsyndromic Hypotrichosis NGS Panel

Fulgent Genetics
United States
2410
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RPL21 Single Gene

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

Results: 1 to 13 of 13

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.