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Results: 1 to 10 of 10

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
971680
  • D Deletion/duplication analysis

Invitae Brain Malformations Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
247161
  • D Deletion/duplication analysis

Sotos syndrome 3, 617169, Autosomal recessive; SOTOS3 (Sotos syndrome) (APC2 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Sotos syndrome 3, 617169, Autosomal recessive; SOTOS3 (Sotos syndrome) (APC2 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

Sotos syndrome and related disorders NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
54
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Sotos syndrome and related disorders Deletion/Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
54
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sotos syndrome and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
54
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Sotos syndrome panel. Panel NGS genes: APC2, NFIX, NSD1.

Genologica Medica
Spain
53
  • C Sequence analysis of the entire coding region

Sotos syndrome panel

Genologica Medica
Spain
53
  • C Sequence analysis of the entire coding region

Sotos syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
33
  • C Sequence analysis of the entire coding region

Results: 1 to 10 of 10

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