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Qualitätssicherung

Qualitätssicherung

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

Jahr Name des Ringversuchs Organisation
Mai 2019ATP7BRfB
Mai 2019ApoERfB
Mai 2019ApoB100RfB
Mai 2019Aldolase BRfB
Mai 2019HFE (Hereditary Haemochromatosis)RfB
Mai 2019LCT (lactose intolerance)RfB
Mai 2019SERPINA1RfB
Mai 2019MTHFR (Homocystinuria)RfB
Mai 2019Prothrombin 20210RfB
Mai 2019Faktor V (Leiden)RfB
Mai 2019CYP2D6RfB
Mai 2019HLA B27RfB
Nov 2018CFTRINSTAND
Nov 2018BRCA1 / BRCA2INSTAND
Nov 2018GJB2INSTAND
Nov 2018MLH1/MSH2INSTAND
Nov 2018DystrophinINSTAND
Nov 2018HTTINSTAND
Nov 2018SMN1INSTAND
Nov 2018CYP21A2INSTAND
Okt 2018ApoERfB
Okt 2018ApoB100RfB
Okt 2018Aldolase BRfB
Okt 2018HFE (Hereditary Haemochromatosis)RfB
Okt 2018LCT (lactose intolerance)RfB
Okt 2018SERPINA1RfB
Okt 2018MTHFR (Homocystinuria)RfB
Okt 2018Prothrombin 20210RfB
Okt 2018Faktor V (Leiden)RfB
Okt 2018HLA B27RfB
Okt 2018DPD Exon 14 skippingRfB
Okt 2018Classification of variants (trial)GenQA
Aug 2018Classification of BRCA1 and BRCA2 variantsEMQN/GenQA
Jul 2018HRF (Hereditary Recurrent Fevers)EMQN
Apr 2018Faktor V (Leiden)RfB
Apr 2018Prothrombin 20210RfB
Apr 2018MTHFR (Homocystinuria)RfB
Apr 2018SERPINA1RfB
Apr 2018ApoERfB
Apr 2018ApoB100RfB
Apr 2018Aldolase BRfB
Apr 2018HFE (Hereditary Haemochromatosis)RfB
Apr 2018LCT (lactose intolerance)RfB
Apr 2018ATP7B (Morbus Wilson)RfB
Apr 2018HLA B27RfB
Apr 2018CYP2D6RfB
Nov 2017Classification of BRCA1 and BRCA2 variantsUK NEQAS
Okt 2017Faktor V (Leiden)RfB
Okt 2017Prothrombin 20210RfB
Okt 2017MTHFR (Homocystinuria)RfB
Okt 2017SERPINA1RfB
Okt 2017ApoERfB
Okt 2017ApoB100RfB
Okt 2017Aldolase BRfB
Okt 2017HFE (Hereditary Haemochromatosis)RfB
Okt 2017LCT (lactose intolerance)RfB
Okt 2017HLA B27RfB
Okt 2017CYP2D6RfB
Okt 2017CYP21A2INSTAND
Okt 2017CFTRINSTAND
Okt 2017BRCA1 / BRCA2INSTAND
Okt 2017GJB2INSTAND
Okt 2017MLH1/MSH2INSTAND
Okt 2017DystrophinINSTAND
Okt 2017HTTINSTAND
Okt 2017SMN1INSTAND
Mai 2017ABCA4Probenaustausch
Mai 2017RS1Probenaustausch
Mai 2017PRPH2Probenaustausch
Mai 2017Faktor V (Leiden)RfB
Mai 2017Prothrombin 20210RfB
Mai 2017HFE (Hereditary Haemochromatosis)RfB
Mai 2017ApoB100RfB
Mai 2017ApoERfB
Mai 2017SERPINA1RfB
Mai 2017LCT (lactose intolerance)RfB
Mai 2017HLA B27RfB
Mai 2017CYP2D6RfB
Mai 2017MTHFR (Homocystinuria)RfB
Mai 2017Aldolase BRfB
Mai 2017ATP7B (Morbus Wilson)RfB
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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