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Results: 1 to 8 of 8

Tests names and labsConditionsGenes, analytes, and microbesMethods

Mental retardation, X-linked 12/35, 300957, X-linked recessive (X-linked intellectual disability-short stature-overweight syndrome) (THOC2 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

Mental retardation, X-linked 12/35, 300957, X-linked recessive (X-linked intellectual disability-short stature-overweight syndrome) (THOC2 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

THOC2 - NGS including CNV analysis

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

Diabetes and Obesity Panel

Centogene AG - the Rare Disease Company
Germany
247262
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
327300
  • C Sequence analysis of the entire coding region

X-Linked Intellectual Disability Panel

PreventionGenetics, part of Exact Sciences
United States
191141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

OmniSeek Whole Exome Sequencing

Juno Genomics Hangzhou Juno Genomics, Inc
China
1041
  • T Targeted variant analysis

Mental retardation, nonsyndromic, X-linked: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
3231
  • C Sequence analysis of the entire coding region

Results: 1 to 8 of 8

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