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  2. Lissencephaly (Tubulin alpha 1A gene)

Lissencephaly (Tubulin alpha 1A gene)

Genetic test Export to PDF
Full name:
Lissencephaly (Tubulin alpha 1A gene)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Mutation confirmation,
Post-natal Diagnosis,
Pre-implantation genetic diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi
Method category:
Sequence analysis: entire coding region
Mutation screening and sequence analysis of selected exons
Method technique:
Bi-directional Sanger Sequence analysis
Laboratory:
Centrum Medische Genetica - UZ Brussel VUB
RIZIV code:
565456-565460
EQA:
  • 2015 DNA Sequencing - Sanger EMQN
  • 2016 DNA Sequencing - Sanger EMQN
  • 2017 DNA Sequencing - Sanger EMQN
  • 2018 DNA Sequencing - Sanger EMQN
  • 2019 DNA Sequencing - Sanger EMQN
  • 2020 DNA Sequencing - Sanger EMQN
  • 2021 DNA Sequencing - Sanger EMQN
  • 2022 DNA Sequencing - Sanger EMQN
Accreditation (ISO 15189):
2021-10-07 / 2026-06-14
Turnaround time (maximum):
3 months
Document(s):
Created:
26 Aug 2019 - 12:22
Changed:
09 Mar 2023 - 16:02
URL:
https://laboguide.uzbrussel.be/laboguide#Analyses:&&5&21&&1067&COLLECTION&3