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Results: 1 to 10 of 10

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Skeletal Disorders Panel

Invitae
United States
624349
  • D Deletion/duplication analysis

Invitae Limb and Digital Malformations Panel

Invitae
United States
356177
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Multiple synostoses syndrome 3, 612961, Autosomal dominant; SYNS3 (Multiple synostoses syndrome) (FGF9 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

Multiple synostoses syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

Multiple Synostosis Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 6 Genes

Reference Laboratory Genetics
Spain
66
  • C Sequence analysis of the entire coding region

SYNOSTOSIS, MULTIPLE

Laboratorio de Genetica Clinica SL
Spain
33
  • C Sequence analysis of the entire coding region

Multiple Synostosis Syndrome Type 3 , Sequencing FGF9 Gene

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

Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked

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

FGF9 Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 10 of 10

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