U.S. flag

An official website of the United States government

GTR Home > Tests > Spinocerebellar ataxia, autosomal recessive 1, 606002, Autosomal recessive (Spinocerebellar ataxia with axonal neuropathy type 2) (MLPA)

Laboratory contact

Laboratory information

Help

Intergen, INTERGEN, Intergen
Intergen Genetics and Rare Diseases Diagnosis Center

Laboratory director(s)

Help
  • G├╝lay Ceylaner, PhD, MD, Lab Director
  • Serdar Ceylaner, MD, Lab Director

Laboratory contact

Help
  • Mustafa Kemal Mh 2119 sk No:5
  • Ankara, Ankara 06510
  • Turkey

Laboratory services offered

Help
  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Confirmation of research findings
  • Custom Balanced Chromosome Rearrangement Studies
  • Custom Deletion/Duplication Testing
  • Custom Prenatal Testing
  • Custom mutation-specific/Carrier testing
  • Cytogenetic testing
  • Genetic counseling
  • Identity Testing
  • Marker Chromosome Identification
  • Maternal cell contamination study (MCC)
  • Mutation Confirmation
  • Preimplantation Genetic Diagnosis (PGD)
  • Rare disease clinical evaluation
  • Rare disease custom testing
  • Result interpretation
  • Uniparental Disomy (UPD) Testing
  • Whole Exome Sequencing
  • Whole Genome Sequencing

Laboratory credentials

Certifications

Help
  • EMQN, Number: 0595, Expiration: 2008-09-28
  • Turkish Ministry of Heath Cytogenetics License, Number: 11379, Expiration: 2010-03-18
  • Turkish Ministry of Heath Molecular Genetics License, Number: 11379, Expiration: 2010-03-18
  • CEQAS, Number: 0595, Expiration: 2021-05-31

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.