Neurogenetics

Neurogenetics
Cyprus Institute of Neurology and Genetics (CING)
Department: Neurogenetics
Iroon Avenue 6
Ayios Dhometios, Nicosia, Cyprus 2371
Phone: +357 22392649
Fax: +357 22392615
Email: roula@cing.ac.cy
Online Contact: https://www.cing.ac.cy/en/about-us/biomedical-sciences-/nd/nd-services
Website: https://www.cing.ac.cy/en/about-us/biomedical-sciences-/nd/nd-services
Affiliated with:
- The Cyprus Institute of Neurology and Genetics, https://www.cing.ac.cy/

Submissions in ClinVar
This is one of your preferred labs. Add to preferred labs, See all preferred labs

GTR Lab ID: 78596, Last updated:2024-09-04

Personnel

Director: Kyproula Christodoulou, PhD, Lab Director
Phone: +357 22392649
Fax: +357 22392615
Email: roula@cing.ac.cy

Conditions and tests

37 conditions/phenotypes with 40 tests
Enter text to narrow down the list

Amyloidosis, hereditary systemic 12 tests
Amyotrophic lateral sclerosis type 11 test
Amyotrophic lateral sclerosis type 101 test
Amyotrophic lateral sclerosis type 61 test
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia1 test
Autosomal dominant Parkinson disease 81 test
Azorean disease2 tests
Charcot-Marie-Tooth disease type 1B1 test
Charcot-Marie-Tooth disease type 1D1 test
Charcot-Marie-Tooth disease type 1E1 test
Charcot-Marie-Tooth disease type 1F1 test
Charcot-Marie-Tooth disease type 2A21 test
Charcot-Marie-Tooth disease type 2B11 test
Charcot-Marie-Tooth disease X-linked dominant 11 test
Charcot-Marie-Tooth disease, type IA1 test
Charcot-Marie-Tooth Neuropathy Type 2H/2K1 test
Dentatorubral-pallidoluysian atrophy1 test
Duchenne and Becker muscular dystrophy1 test
Friedreich ataxia 11 test
Hereditary spastic paraplegia 311 test
Hereditary spastic paraplegia 3A2 tests
Hereditary spastic paraplegia 42 tests
Hereditary spastic paraplegia 441 test
Huntington disease1 test
Kennedy disease1 test
Neuronopathy, distal hereditary motor, autosomal recessive 51 test
Neuronopathy, distal hereditary motor, type 5A1 test
Spinal muscular atrophy1 test
Spinocerebellar ataxia 72 tests
Spinocerebellar ataxia type 12 tests
Spinocerebellar ataxia type 101 test
Spinocerebellar ataxia type 121 test
Spinocerebellar ataxia type 171 test
Spinocerebellar ataxia type 22 tests
Spinocerebellar ataxia type 62 tests
Spinocerebellar ataxia type 81 test
Steinert myotonic dystrophy syndrome1 test

List of services

Clinical Testing/Confirmation of Mutations Identified Previously: Order Code: 1, 6.11, 8, 24, 26, 70, 83
Custom Sequence Analysis: Order Code: 1.01, 20, 6.02, 6.03, 6.04, 6.06, 6.07, 6.08, 6.09, 6.10, 23, 25
Repeat Expansion Testing: Order Code: 2, 3, 4, 5, 12, 13, 14, 15, 16, 17, 18, 19, 21, 22, 33, 72, 73,
WES based in silico gene panels: Order Code: 40.2, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55
Custom Deletion/Duplication Testing: Order Code: 6.05, 7.01, 30, 71,
Whole Exome Sequencing: Order Code: 64, 65
Confirmation of research findings: Order Code: 83

List of certifications/licenses

Certifications

ISO15189, Number: L061-3, Expiration date: 2026-06-19

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.