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Labor Dr. Wisplinghoff

  • laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
  • Horbeller Str. 18-20
  • 50858 KÖLN
  • GERMANIA
  • Stato : Private for-profit
  • Telefono : 49 (0)221 940 505 0
  • Altro telefono : -
  • Fax : 49 (0)221 940 505 950
  • Sito web
  • Numero EUGT : EUGTDE376747

Contatti

Gestione della qualità

Accreditato							
 Accreditamento

Accreditamento
Ente
Anno
Ambito dell’accreditamento

VEQ VEQ

VEQ elencate per EMQN

BRAF (Molecular testing for malignant melanoma)
2016, 2017, 2018, 2019
BRCA (Familial breast cancer) - genotyping
2015
CMT/HNPP (Charcot-Marie-Tooth disease / Hereditary Neuropathy with Pressure Palsies)
2015, 2017, 2018, 2019
Cell-free DNA (cfDNA) for EGFR gene mutations in Lung Cancer
2018
DFNB1 (Hereditary Deafness)
2015, 2016, 2017, 2018, 2019
EGFR (Molecular testing for non small cell lung cancer)
2016, 2017, 2018, 2019
FAP (Familial Adenomatous Polyposis Colon Cancer)
2015, 2017, 2018, 2019
FH (Familial hypercholesterolemia - pilot scheme)
2015, 2017, 2018, 2019
FRAX (Fragile X syndrome) - full scheme
2017, 2018, 2019
Germline NGS mutation testing
2017, 2018, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2016, 2017, 2018, 2019
HNPCC (Hereditary non-polyposis colon cancer)
2015, 2016, 2017, 2018
HRF (Hereditary Recurrent Fevers)
2016, 2017, 2019
KRAS (Molecular testing for sporadic colorectal cancer)
2016, 2017, 2018, 2019
Molecular testing of germline changes in BRCA genes for ovarian cancer
2017, 2018, 2019
Molecular testing of somatic changes in BRCA genes for ovarian cancer
2016, 2017, 2018, 2019
MonoDiab (Monogenic Diabetes)
2015, 2016, 2017, 2018, 2019
Multiplex oncology pilot EQA
2018
Non-invasive prenatal testing (NIPT) for common aneuploidies
2017, 2018, 2019
Non-invasive prenatal testing (NIPT) for fetal sexing
2019
ONCOPANEL (Oncogene panel testing) - pilot scheme
2017, 2018, 2019
PWAS (Prader-Willi and Angelman syndromes)
2017, 2018, 2019
SCA (Spinocerebellar ataxias)
2018, 2019
SEQ (DNA sequencing) - Full scheme
2017, 2018, 2019
SHOX (Short stature homeobox gene testing)
2015, 2016, 2017, 2018
Somatic NGS mutation testing
2016, 2017, 2018, 2019
VHL (Von Hippel Lindau syndrome)
2017, 2018, 2019
aCGH/ Microarrays
2016, 2017, 2018, 2019

VEQ elencate per INSTAND

Molekulargenetik I (Faktor V-Leiden-Mutation)
2016
Molekulargenetik I (MTHFR)
2016
Molekulargenetik I (PAI-1 4G/5G)
2016
Molekulargenetik I (Prothrombin 20210)
2016
Molekulargenetik II (Apolipoprotein E : E2, E3, E4)
2016
Molekulargenetik II (HFE)
2016
Molekulargenetik SET 01 (Faktor VII)
2016
Molekulargenetik SET 02 (APOB 100: R3500Q)
2016
Molekulargenetik SET 02 (a1-AT)
2016
Molekulargenetik SET 03 (BCHE)
2016
Molekulargenetik SET 03 (HLA-B27)
2016
Molekulargenetik SET 05 (NOD2)
2016
Molekulargenetik SET 06 (CYP2C9)
2016
Molekulargenetik SET 06 (FSHR)
2016
Molekulargenetik SET 06 (TPMT)
2016
Molekulargenetik SET 07 (KRAS)
2016
Molekulargenetik SET 08 (CYP2D6)
2016
Molekulargenetik SET 08 (DPD: Exon 14 skipping)
2016
Molekulargenetik SET 08 (VKORC1)
2016
Molekulargenetik SET 09 (CFTR)
2016
Molekulargenetik SET 12 (FMR1)
2016
Molekulargenetik SET 14 (MSH2, MLH1)
2016
Molekulargenetik SET 15 (HTT)
2016
Molekulargenetik SET 16 (SNRPN)
2016
Molekulargenetik SET 17 (SMN1)
2016
Molekulargenetik SET 18 (Y-Chromosom AZF)
2016
Molekulargenetik SET 19 (BRCA1)
2016
Molekulargenetik SET 20 (alpha globin)
2016
Molekulargenetik SET 20 (beta globin)
2016
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.