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Results: 1 to 19 of 19

Tests names and labsConditionsGenes and analytesMethods

Osteopetrosis, autosomal recessive 7 - Sanger / Del Dup Comprehensive

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Osteopetrosis, autosomal recessive 7 (OPTB7) - Deletion/Duplication

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis

Osteopetrosis, autosomal recessive 7 (OPTB7) - Sanger Sequencing

Connective Tissue Gene Tests
United States
11
  • C Sequence analysis of the entire coding region

Osteopetrosis autosomal recessive type 7

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

Low Bone Mass Panel (MitomeNGS)

Baylor Miraca Genetics Laboratories
United States
3922
  • C Sequence analysis of the entire coding region

TNFRSF11A Comprehensive - Sequence & Deletion/Duplication Analysis

Baylor Miraca Genetics Laboratories
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TNFRSF11A Deletion/Duplication Analysis

Baylor Miraca Genetics Laboratories
United States
31
  • D Deletion/duplication analysis

TNFRSF11A Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
31
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TNFRSF11A Sequence Analysis (Prenatal Diagnosis)

Baylor Miraca Genetics Laboratories
United States
31
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
845637
  • D Deletion/duplication analysis

Paget Disease of Bone, Autosomal Recessive Osteopetrosis, and Familial Expansile Osteolysis via the TNFRSF11A Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

OSTEOPETROSIS

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
108
  • C Sequence analysis of the entire coding region

Skeletal dysplasia with increased bone density Panel

CeGaT GmbH
Germany
2628
  • C Sequence analysis of the entire coding region

TNFRSF11A

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
371161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paget Disease of Bone NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
365163
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia With Increased Bone Density: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
4522
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta and Decreased Bone Density: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
8134
  • C Sequence analysis of the entire coding region

Results: 1 to 19 of 19

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