Orphanet: Centrum voor Medische Genetica
x

Zoek een instelling

*(*) verplicht veld

Centrum voor Medische Genetica

  • UZ Gent
  • Center for Medical Genetics Gent
  • C. Heymanslaan 10 (Entrance 34 (Medical Research Building))
  • 9000 GENT
  • BELGI╦
  • Status : -
  • Telefoon : +32 (0)9 332 36 03
  • Aanvullend telefoonnummer : -
  • Fax : +32 (0)9 332 49 70
  • Website
  • Contacteer het secretariaat
  • EUGT-nummer : EUGTBE56112

Kwaliteitsbeheer

Accreditatie
 Accreditatie

Accreditatie
Accreditatie-instelling
Jaar
Accreditatie scope

EQA
 EQA

EQA schema(s) georganiseerd door CEQAS

Acquired array exploratory pilot and survey
2014
Acquired microarray
2016
Acute Lymphoblastic Leukaemia
2016
Blood - Postnatal
2015, 2017
CNS (Central Nervous system) Tumours
2017
Constitutional microarray (postnatal)
2015, 2017
MRA (Molecular Rapid Aneuploidy - QF-PCR/MLPA)
2016
Myeloid Leukaemia (AML; MDS; CML)
2015, 2017
Myeloma
2017
Myeloma exploratory pilot and survey
2015
NIPT exploratory pilot
2016, 2017
PGD Blastomere/Trophectoderm array/NGS for aneuploidy pilot
2016, 2017
PGD Blastomere/Trophectoderm array/NGS for translocations pilot
2016, 2017
Pilot PGD microarray blastomere/trophectoderm
2014
Pilot Products of conception (Array/MLPA/PCR)
2014
Prenatal array exploratory pilot and survey
2014
Prenatal microarray
2016
Products of conception (Array/MLPA/QF-PCR/NGS)
2017

EQA schema(s) georganiseerd door CF Network

CF (Cystic fibrosis)
2016, 2018

EQA schema(s) georganiseerd door EMQN

ADPKD (Autosomal dominant polycystic kidney disease)
2015, 2016, 2018
AZF (Y-Chromosome microdeletions)
2017, 2018, 2019
CMT/HNPP (Charcot-Marie-Tooth disease / Hereditary Neuropathy with Pressure Palsies)
2015, 2015, 2017, 2019
CMT/HNPP (Charcot-Marie-Tooth disease) / Hereditary Neuropathy with Pressure Palsies
2017
DFNB1 (Hereditary Deafness)
2015, 2017, 2019
DM (Myotonic dystrophy)
2015, 2017, 2019
FAP (Familial Adenomatous Polyposis Colon Cancer)
2015, 2018
FRAX (Fragile X syndrome) - full scheme
2016, 2018
Germline NGS mutation testing
2016, 2018, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2016, 2018
HD (Huntington disease)
2015, 2017, 2019
HFE (Hereditary hemochromatosis)
2017, 2019
HNPCC (Hereditary non-polyposis colon cancer)
2015, 2017, 2019
MEN2 (Multiple Endocrine Neoplasia Type 2)
2015, 2018
Molecular testing of germline changes in BRCA genes for ovarian cancer
2018
Molecular testing of somatic changes in BRCA genes for ovarian cancer
2017, 2018, 2019
Multiplex oncology pilot EQA
2018
NextGen DNA Sequencing (vGermline)
2016
NextGen DNA Sequencing (vSomatic)
2016
Non-invasive prenatal diagnosis-Pilot EQA scheme
2015
OI (Osteogenesis imperfecta)
2015, 2017, 2019
PWAS (Prader-Willi and Angelman syndromes)
2016, 2018, 2018
SEQ (DNA sequencing) - Full scheme
2015, 2016, 2017, 2018, 2019
SHOX (Short stature homeobox gene testing)
2015, 2017, 2019
SMA (Spinal muscular atrophy)
2016, 2018
Somatic NGS mutation testing
2016, 2018
VHL (Von Hippel-Lindau syndrome)
2014, 2016, 2018
cffDNA (Cell free fetal DNA for sex determination)
2015

EQA schema(s) georganiseerd door GenQA

Lymphoblastic Leukaemia (ALL)
2018
Molecular Rapid Aneuploidy (MRA)
2018
Myeloid (AML/MDS/CML)
2018
Myeloma
2018
Non-invasive prenatal testing for common aneuploidies pilot
2018
Preimplantation Genetic Testing by NGS and/or arrays for trophectoderm and/or blastomere testing for chromosomal rearrangements
2018
Preimplantation Genetic Testing for monogenic disorders Stage 1
2018
Preimplantation Genetic Testing for monogenic disorders Stage 2
2018
Prenatal constitutional CNV detection (previously Prenatal microarray)
2018
Severe Intellectual Disability Interpretation Case Scenario pilot
2018
De documenten op deze website zijn louter ter informatie. Het materiaal is geenszins bestemd om professionele medische zorgen door een gediplomeerde specialist te vervangen en mag niet worden gebruikt als basis voor een diagnose of behandeling.