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Results: 1 to 12 of 12

Tests names and labsConditionsGenes and analytesMethods

Hyaline fibromatosis syndrome

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

Hyaline Fibromatosis Syndrome via the ANTXR2 Gene

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

ANTXR2. Complete sequencing

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

Congenital Contractures Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
8557
  • C Sequence analysis of the entire coding region

Juvenile Hyaline Fibromatosis, Sequencing ANTXR2 Gene

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

JUVENILE HYALINE FIBROMATOSIS

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Juvenile hyaline fibromatosis

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

Lysosomal Storage Disease Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
6775
  • C Sequence analysis of the entire coding region

ANTXR2

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

Lysosomal Disorders NGS Panel

Fulgent Genetics
United States
193106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyalinosis, Inherited Systemic (sequence analysis of ANTXR2 gene)

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

CMG2 (ANTXR2) - Hyalinosis, Infantile Systemic

Centre of Molecular Diseases (CMM) CHUV
Switzerland
11
  • C Sequence analysis of the entire coding region

Results: 1 to 12 of 12

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