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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Beaulieu-Boycott-Innes syndrome, 613680, Autosomal recessive; BBIS (Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type) (THOC6 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

Beaulieu-Boycott-Innes syndrome, 613680, Autosomal recessive; BBIS (Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type) (THOC6 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

Beaulieu-Boycott-Innes syndrome: Full gene sequencing

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

THOC6 Single Gene

Fulgent Genetics
United States
191
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microcephaly NGS Panel

Fulgent Genetics
United States
32275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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