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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hydrocephalus Panel

PreventionGenetics, part of Exact Sciences
United States
4138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, 300863, X-linked dominant (X-linked dominant chondrodysplasia, Chassaing-Lacombe type) (HDAC6 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

Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, 300863, X-linked dominant (X-linked dominant chondrodysplasia, Chassaing-Lacombe type) (HDAC6 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

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

Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

HDAC6 Single Gene

Fulgent Genetics
United States
341
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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