Filters

See more specimen types...

Other countries

Results: 1 to 19 of 19

Tests names and labsConditionsGenes and analytesMethods

Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection

PreventionGenetics
United States
327258
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GALNT3-Related Disorders via the GALNT3 Gene

PreventionGenetics
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

ExomePLUS Electrolyte & Kidney Stone

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
4649
  • C Sequence analysis of the entire coding region

GALNT3. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
8465
  • D Deletion/duplication analysis

Hereditary kidney disorders - different panels

Institute of Human Genetics Cologne University
Germany
28411
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hyperphosphatemic Tumoral Calcinosis , Sequencing GALNT3 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

GALNT3

Fulgent Genetics
United States
141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital disorder of O-linked glycosylation (CDG)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3929
  • C Sequence analysis of the entire coding region

Tumoral calcinosis, hyperphosphatemic: GALNT3 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Tumoral calcinosis

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

Tumoral calcinosis, hyperphosphatemic (sequence analysis of GALNT3 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Single gene testing GALNT3

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Tumoral calcinosis, hyperphosphatemic, familial

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS panel

Fulgent Genetics
United States
370161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
364163
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia With Increased Bone Density: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
4522
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
8566
  • C Sequence analysis of the entire coding region

Hyperphosphatemic Familial Tumoral Calcinosis, GALNT3-Related

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 1 to 19 of 19

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.

Support Center