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Results: 1 to 20 of 200

Tests names and labsConditionsGenes, analytes, and microbesMethods

Retinoblastoma

Genetic Pathology SA Pathology
Australia
21
  • S Multicolor FISH (M-FISH)/Spectral Karyotyping™ (SKY™)
  • D Deletion/duplication analysis
  • H Detection of homozygosity
  • M Methylation analysis
  • C Sequence analysis of the entire coding region

Retinoblastoma, 180200, Autosomal dominant, Somatic mutation; RB1 (Retinoblastoma) (RB1 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

Retinoblastoma, trilateral, 180200, Autosomal dominant, Somatic mutation; RB1; RB1 (Retinoblastoma) (RB1 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

Retinoblastoma

Genologica Medica
Spain
41
  • C Sequence analysis of the entire coding region

Retinoblastoma

Genologica Medica
Spain
41
  • C Sequence analysis of the entire coding region

Retinoblastoma

Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine
United States
11
  • D Deletion/duplication analysis
  • M Methylation analysis
  • C Sequence analysis of the entire coding region

Retinoblastoma

IUMS Hospital Medical Genetics Lab Iran University of Medical Sciences
Iran
11
  • E Sequence analysis of select exons

Retinoblastoma

Molecular Genetics Laboratory North York General Hospital
Canada
11
  • C Sequence analysis of the entire coding region

Genetic testing in retinoblastoma

Eye Cancer Genetics Universitätsklinikum Essen
Germany
21
  • D Deletion/duplication analysis
  • L Linkage analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

RETINOBLASTOMA

Laboratorio de Genetica Clinica SL
Spain
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinoblastoma

Asper Biogene Asper Biogene LLC
Estonia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinoblastoma

Mendelics
Brazil
11
  • C Sequence analysis of the entire coding region

Retinoblastoma

Bioarray
Spain
11
  • D Deletion/duplication analysis

Retinoblastoma

Laboratory of Human Genetics GENOMED Health Care Center
Poland
11
  • C Sequence analysis of the entire coding region

Retinoblastoma

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • M FISH-metaphase
  • D Deletion/duplication analysis
  • L Linkage analysis
  • S Mutation scanning of the entire coding region

Retinoblastoma

Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab)
United States
11
  • I FISH-interphase
  • M FISH-metaphase

Retinoblastoma

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • M FISH-metaphase

Retinoblastoma

Center for Human Genetics Laboratory University Hospitals - University Hospitals Laboratory Service Foundation
United States
11
  • I FISH-interphase
  • M FISH-metaphase

RB1 testing for Retinoblastoma

Impact Genetics Dynacare/LabCorp
Canada
32
  • D Deletion/duplication analysis
  • M Methylation analysis
  • X Mutation scanning of select exons
  • R RNA analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Retinoblastoma

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Results: 1 to 20 of 200

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.