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Results: 21 to 33 of 33

Tests names and labsConditionsGenes, analytes, and microbesMethods

Congenital Stationary Night Blindness (CSNB) NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1715
  • C Sequence analysis of the entire coding region

NIGHT BLINDNESS, CONGENITAL STATIONARY (X-LINKED)

Laboratorio de Genetica Clinica SL
Spain
22
  • C Sequence analysis of the entire coding region

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
367291
  • C Sequence analysis of the entire coding region

Single gene testing CACNA1F

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

Cone Rod Dystrophy panel

Molecular Vision Laboratory
United States
5133
  • C Sequence analysis of the entire coding region

Congenital Stationary Night Blindness panel

Molecular Vision Laboratory
United States
1914
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372283
  • C Sequence analysis of the entire coding region

CACNA1F Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Stationary Night Blindness

Asper Biogene Asper Biogene LLC
Estonia
1010
  • 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

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cone-Rod Dystrophy NGS Panel

Fulgent Genetics
United States
5629
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 33 of 33

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