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Results: 1 to 15 of 15 (representing 6 labs)

Tests names and labsConditionsGenes and analytesMethods

Leukemia, promyelocytic acute form

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leukemia, acute promyelocytic form

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RARA

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

NUMA1

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Detection by FISH of t(15;17) PML/RARA

CGC Genetics
Portugal
12
  • F Fluorescence in situ hybridization (FISH)

Detection by FISH of RARA (17q21) rearrangements

CGC Genetics
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

Detection by FISH of TP53 (17p13.1) deletion/amplification

CGC Genetics
Portugal
21
  • I FISH-interphase

RT-PCR t(5;17)(q35;q21) NPM/RARA

CGC Genetics
Portugal
12
  • R RNA analysis

RT-PCR t(15;17)(PML/RARa)

CGC Genetics
Portugal
12
  • R RNA analysis

RT-PCR t(11;17)

CGC Genetics
Portugal
12
  • R RNA analysis

PML/RARa fusion gene quantification

CGC Genetics
Portugal
12
  • T Targeted variant analysis

Leukemia, acute promyelocytic, NUMA/RARA type (sequence analysis of NUMA1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leukemia, acute promyelocytic, PML/RARA type (sequence analysis of PML gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Chromosome Analysis: Cancer

Genomic Research Center Shahid Beheshti University of Medical Sciences
Iran
111
  • K Karyotyping

Chromosome Analysis: Cancer

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
251
  • K Karyotyping

Results: 1 to 15 of 15

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.

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