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Results: 1 to 20 of 36

Tests names and labsConditionsGenes, analytes, and microbesMethods

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

CFHR1 - MLPA

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis

CFHR3 - MLPA

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis

Invitae Macular Dystrophy Panel

Invitae
United States
6636
  • D Deletion/duplication analysis

Macular degeneration, age-related, reduced risk of, 603075, Autosomal dominant (CFHR1 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

Macular degeneration, age-related, 1, 603075, Autosomal dominant; ARMD1 (HMCN1 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

Macular degeneration, age-related, 603075, Autosomal dominant (APOE 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

Macular degeneration, age-related, reduced risk of, 603075, Autosomal dominant (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Macular degeneration, age-related, reduced risk of, 603075, Autosomal dominant (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Macular degeneration, age-related, reduced risk of, 603075, Autosomal dominant (CFHR3 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

RenalZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital
United States
527338
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
342268
  • C Sequence analysis of the entire coding region

Stargardt Disease (STGD) and Macular Dystrophies Panel

PreventionGenetics, Part of Exact Sciences
United States
3528
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dyslipidemia and early atherosclerosis panel. 84-gene NGS panel.

Genologica Medica
Spain
13384
  • C Sequence analysis of the entire coding region

Alzheimer's panel

Genologica Medica
Spain
2510
  • C Sequence analysis of the entire coding region

Familial hypercholesterolemia panel. 16-gene NGS panel.

Genologica Medica
Spain
2016
  • C Sequence analysis of the entire coding region

Dementia panel. NGS panel of 21 genes.

Genologica Medica
Spain
4421
  • C Sequence analysis of the entire coding region

Hyperlipidemia panel. 18-gene NGS panel.

Genologica Medica
Spain
2518
  • C Sequence analysis of the entire coding region

Alzheimer's panel. NGS panel of 10 genes.

Genologica Medica
Spain
2510
  • C Sequence analysis of the entire coding region

Complement Deficiency panel

Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
2833
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 36

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