Orphanet: Laboratoire de Génétique moléculaire
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Cerca un istituto

*(*) campo obbligatorio

Laboratoire de Gntique molculaire

  • Centre de Gntique Humaine (CGH) de l'UCL/Center for Clinical Genetics of the Saint-Luc hospital
  • Cliniques Universitaires UCL Saint-Luc
  • Avenue Hippocrate, 10
  • 1200 BRUSSELS
  • BELGIO
  • Stato : Public
  • Telefono : +32 (0)2 764 67 74
  • Altro telefono : -
  • Fax : +32 (0)2 764 69 36
  • Sito web
  • email di contatto
  • Numero EUGT : EUGTBE418741

Contatti

Gestione della qualit

Accreditato
 Accreditamento

Accreditamento
Ente
Anno
Ambito dellaccreditamento

VEQ
 VEQ

VEQ elencate per CF Network

CF (Cystic fibrosis)
2015, 2016, 2017, 2018, 2019

VEQ elencate per EMQN

11p-Imprinting Disorder Scheme (BWS/SRS)
2016, 2019
AZF (Y-Chromosome microdeletions)
2015, 2017, 2018, 2019
BWS (Beckwith-Wiedemann syndrome)
2015
DFNB1 (Hereditary Deafness)
2015, 2016, 2017, 2018, 2019
FAP (Familial Adenomatous Polyposis Colon Cancer)
2017, 2018, 2019
FRAX (Fragile X syndrome) - full scheme
2015, 2016, 2017, 2018, 2019
Germline NGS mutation testing
2015, 2016, 2017, 2018, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2017, 2019
HD (Huntington disease)
2015, 2016, 2017, 2018
HFE (Hereditary hemochromatosis)
2015, 2016, 2017, 2018, 2019
HNPCC (Hereditary non-polyposis colon cancer)
2017, 2018, 2019
MEN2 (Multiple Endocrine Neoplasia Type 2)
2019
Molecular testing of somatic changes in BRCA genes for ovaria cancer
2019
PWAS (Prader-Willi and Angelman syndromes)
2015, 2016, 2017, 2018
SEQ (DNA sequencing) - Full scheme
2014, 2015, 2016, 2017, 2018, 2019
SMA (Spinal muscular atrophy)
2015, 2018
VHL (Von Hippel Lindau syndrome)
2015, 2017, 2018, 2019
Tutte le informazioni presenti nel sito non sostituiscono in alcun modo il giudizio di un medico specialista, l'unico autorizzato ad effettuare una consulenza medica ed esprimere un parere medico.