Orphanet: D�partement de G�n�tique Clinique Institut de Pathologie et de G�n�tique IPG
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Dpartement de Gntique Clinique - Institut de Pathologie et de Gntique (IPG)

  • Institut de Pathologie et de Gntique
  • Avenue Georges Lematre, 25
  • 6041 GOSSELIES
  • BELGIUM
  • Status : Private for-profit
  • Phone : +32 (0)71 47 30 47
  • Additional Phone : +32 (0)71 44 71 81
  • Fax : +32 (0)71 34 78 61
  • Website
  • Contact
  • EUGT number : EUGTBE418717

Quality management

Accreditation
 Accreditation

Accreditation
Organism
Year
Accreditation scope

EQA
 EQA

EQA scheme(s) organized by CEQAS

Acquired array exploratory pilot and survey
2014, 2015
Acquired microarray
2016, 2017
Blood - Postnatal
2014, 2015, 2016, 2017
Constitutional microarray (postnatal)
2014, 2015, 2016, 2017
MRA (Molecular Rapid Aneuploidy - QF-PCR/MLPA/BoBs)
2017
Mature B and T neoplasms (G-banding/FISH)
2014
Myeloid Leukaemia (AML; MDS; CML)
2015, 2016
Myeloma
2016
Myeloma exploratory pilot and survey
2015
Prenatal array exploratory pilot and survey
2014, 2015
Prenatal microarray
2016, 2017
Tumour
2016

EQA scheme(s) organized by CF Network

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

EQA scheme(s) organized by EMQN

ADPKD (Autosomal dominant polycystic kidney disease)
2015, 2018
AZF (Y-Chromosome microdeletions)
2017, 2018
CMT/HNPP (Charcot-Marie-Tooth disease / Hereditary Neuropathy with Pressure Palsies)
2017
DFNB1 (Hereditary Deafness)
2015, 2018
DM (Myotonic dystrophy)
2017
DMD (Duchenne and Becker muscular dystrophies)
2015, 2016, 2017, 2018, 2019
FRAX (Fragile X syndrome) - full scheme
2015, 2018
FRDA (Friedreich ataxia)
2015, 2018
Germline NGS mutation testing
2015, 2017, 2018, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2017, 2019
HD (Huntington disease)
2016, 2019
HFE (Hereditary hemochromatosis)
2015, 2018
HNPCC (Hereditary non-polyposis colon cancer)
2016, 2019
MEN2 (Multiple Endocrine Neoplasia Type 2)
2016, 2019
Mitochondrial metabolic disorders
2017, 2018
Molecular testing of germline changes in BRCA genes for ovarian cancer
2016, 2017
Molecular testing of somatic changes in BRCA genes for ovarian cancer
2016, 2017
MonoDiab (Monogenic Diabetes)
2017
Multiplex oncology pilot EQA
2018
Non-invasive prenatal testing (NIPT) for common aneuploidies
2017, 2019
PWAS (Prader-Willi and Angelman syndromes)
2016, 2019
SCA (Spinocerebellar ataxias)
2016, 2017, 2018, 2019
SEQ (DNA sequencing) - Full scheme
2015, 2016, 2017, 2018, 2019
SHOX (Short stature homebox gene testing)
2016, 2019
SMA (Spinal muscular atrophy)
2016, 2019
Somatic NGS mutation testing
2017, 2019
cffDNA (Cell free fetal DNA for sex determination)
2015, 2016

EQA scheme(s) organized by GenQA

Acquired array (CLL/MDS)
2018
Blood - Postnatal
2018
Constitutional microarray (postnatal)
2018
Molecular Rapid Aneuploidy (MRA)
2018
Myeloid (AML/MDS/CML)
2018
Prenatal constitutional CNV detection (previously Prenatal microarray)
2018
Products of Conception/Fetal tissue (Molecular methods)
2018
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.