Qualitätssicherung

Qualitätssicherung

Um die Qualität der Analysen dauerhaft sicherzustellen, nimmt unser Labor regelmäßig an nationalen und internationalen Qualitätssicherungsprogrammen teil.

Jahr Name des Ringversuchs Organisation
Dez 2016TP53INSTAND
Nov 2016Faktor V (Leiden)INSTAND
Nov 2016Prothrombin 20210INSTAND
Sep 2016HFE (Hereditary Haemochromatosis)INSTAND
Sep 2016ApoB100INSTAND
Sep 2016ApoEINSTAND
Sep 2016SERPINA1INSTAND
Sep 2016LCT (lactose intolerance)INSTAND
Sep 2016HLA B27INSTAND
Sep 2016CYP2D6INSTAND
Sep 2016Hb S (sickle cell haemoglobin)INSTAND
Sep 2016DPD (5-fluorouracil toxicity)INSTAND
Sep 2016PRNP (prionopathy)INSTAND
Sep 2016GJB2 (Connexin 26)INSTAND
Sep 2016MSH2 / MLH1 (HNPCC)INSTAND
Sep 2016HTT (Huntington Disease)INSTAND
Sep 2016SMN1 (Spinal muscular atrophy)INSTAND
2016FH (Familial autosomal dominant hypercholesterolemia)EMQN
2016FRDA (Friedreich Ataxia)EMQN
2016MONODIAB (Monogenic Diabetes)EMQN
2016SHOX (Familial SHOX-related disorders)EMQN
2016Wilson DiseaseEMQN
Mai 2016Faktor V (Leiden)INSTAND
Mai 2016Prothrombin 20210INSTAND
Mai 2016HFE (Hereditary Haemochromatosis)INSTAND
Mai 2016ApoB100INSTAND
Mai 2016ApoEINSTAND
Mai 2016SERPINA1INSTAND
Mai 2016LCT (lactose intolerance)INSTAND
Mai 2016HLA B27INSTAND
Mai 2016HLA DQA1 *05/ DQB1*02 / DQB1*03:02INSTAND
Mai 2016CYP21BINSTAND
Mai 2016CYP2D6INSTAND
Mai 2016Hb S (sickle cell haemoglobin)INSTAND
Mai 2016DPD (5-fluorouracil toxicity)INSTAND
Mai 2016PRNP (prionopathy)INSTAND
Mai 2016CFTRINSTAND
Mai 2016BRCA1 / BRCA2INSTAND
Mai 2016Dystrophin (Duchenne / Becker Muscular Dystrophy)INSTAND
2015Faktor V (Leiden)INSTAND
2015Prothrombin 20210INSTAND
2015HFE (Hereditary Haemochromatosis)INSTAND
2015ApoB100INSTAND
2015ApoEINSTAND
2015LCT (lactose intolerance)INSTAND
2015HLA B27INSTAND
2015HLA DQA1 *05/ DQB1*02 / DQB1*03:02INSTAND
2015CYP2D6INSTAND
2015Hb S (sickle cell haemoglobin)INSTAND
2015DPD (5-fluorouracil toxicity)INSTAND
2015PRNP (prionopathy)INSTAND
2015Dystrophin (Duchenne / Becker Muscular Dystrophy)INSTAND
2015GJB2 (Connexin 26)INSTAND
2015HTT (Huntington Disease)INSTAND
2015SMN1 (Spinal muscular atrophy)INSTAND
2015Cystic fibrosisCF network
2015APKD (Autosomal Dominant Polycystic Kidney disease)EMQN
2015BRCA (Full sheme)EMQN
2015CAH (Congenital Adrenal hyperplasia)EMQN
2015HNPCC (Lynch syndrome)EMQN
2015MONODIAB (Monogenic Diabetes)EMQN
2015OI (Osteogenesis Imperfecta)EMQN
2015Wilson DiseaseEMQN
2015Faktor V (Leiden)RfB
2015a1-Proteinase-InhibitorRfB
2015Aldolase BRfB
2015Faktor IIRfB
2015ApoERfB
2015HFE (Hereditary Haemochromatosis)RfB
2015MTHFR (Homocystinuria)RfB
2015ApoB100RfB
2015HLA-B27RfB
2015CYP2D6RfB
2014MONODIAB (Monogenic Diabetes)EMQN
2014SMA (Spinal muscular atrophy)EMQN
2014HFE (Hereditary Haemochromatosis)EMQN
2014BRCA (Full scheme)EMQN
2014DFNB1 (Hereditary Deafness)EMQN
2014DMD (Duchenne / Becker Muscular Dystrophy)EMQN
2014HD (Huntington Disease)EMQN
2014HNPCC (Lynch Syndrome)EMQN
2012HFE (Hereditary Haemochromatosis)EMQN
2012DMD (Duchenne / Becker Muscular Dystrophy)EMQN
2012HNPCC (Lynch syndrome)EMQN
2012HD (Huntington Disease)EMQN
2012BRCA (Full scheme)EMQN
2012DFNB1 (Hereditary Deafness)EMQN
2012SMA (Spinal Muscular Atrophy)EMQN
2011FAP (Familial adenomatous polyposis)EMQN
2011MEN2 (Multiple Endocrine Neoplasia Type 2)EMQN
2011PKU (Phenylketonuria )EMQN
2011SMA (Spinal Muscular Atrophy)EMQN
2010BRCA (Full sheme)EMQN
2010HNPCC (Lynch syndrome)EMQN
2010CMT (Charcot-Marie-Tooth disease)EMQN
2010VHL (Von Hippel Lindau Syndrome)EMQN
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