Abteilung Molekulargenetik
- Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ) Dr. Klein, Dr. Rost und Kollegen
- MVZ Martinsried GmbH
- Lochhamer Str. 29
- 82152 MARTINSRIED/PLANEGG
- GERMANY
- Status : Private for-profit
- Telefon : 49 (0)89 89 55 78 0
- Dodatkowy telefon : -
- Fax : 49 (0)89 89 55 78 780
- Strona internetowa
- Kontakt
email- EUGT number : EUGTDE101794
Kontakt
- Kierownik laboratorium: Dr Imma ROST
- Professionals: Ms Birgit BUSSE, Dr Soheyla CHAHROKH-ZADEH, Dr Hanns-Georg KLEIN, Dr Christoph MARSCHALL, Dr Karin MAYER, Dr Imma ROST, Dr Ralf ZARBOCK
Dane dotyczące zarządzania jakością
Akredytacja
Akredytacja
Organism
Year
Accreditation scope
EQA
EQA scheme(s) organized by CF Network
CF (Cystic fibrosis)
2015, 2016, 2018
EQA scheme(s) organized by DGKL/RfB
ACE
2017
ALDOB
2017
ATP7B-C3207A
2017
Alpha-1-Proteinase-Inhibitor
2017
CETP
2017
COL1A1 Sp1
2017
F VII (R353Q)
2017
HFE
2017
LCTC C13910T
2017
MTHFR
2017
SQ DNA Sequencing
2017
VDR
2017
EQA scheme(s) organized by EMQN
ADPKD (Adult dominant polycystic kidney disease)
2016, 2017, 2018, 2019
AZF (Y-Chromosome microdeletions)
2016, 2017, 2018, 2019
CAH (Congenital Adrenal Hyperplasia)
2016, 2017, 2018, 2019
CMT/HNPP (Charcot-Marie-Tooth disease / Hereditary Neuropathy with Pressure Palsies)
2016, 2017, 2019
Cardiac genetics - arrthymias
2019
DFNB1 (Hereditary Deafness)
2016
DM (Myotonic dystrophy)
2016, 2017, 2019
DMD (Duchenne and Becker muscular dystrophies)
2016
FAP (Familial Adenomatous Polyposis Colon Cancer)
2016, 2017, 2018, 2019
FH (Familial hypercholesterolemia - pilot scheme)
2016, 2017, 2018, 2019
FRAX (Fragile X syndrome) - full scheme
2016
Germline NGS mutation testing
2016, 2017, 2018
HBOC (Hereditary Breast and Ovarian Cancer testing)
2016, 2017, 2018, 2019
HD (Huntington disease)
2016
HFE (Hereditary hemochromatosis)
2018, 2019
HNPCC (Hereditary non-polyposis colon cancer)
2016, 2017, 2018, 2019
HRF (Hereditary Recurrent Fevers)
2016, 2017, 2018, 2019
KRAS (Molecular testing for sporadic colorectal cancer)
2016, 2017, 2018, 2019
Liquid Biopsy (pilot)
2017
Lung Cancer (NSCLC)4
2017
MEN2 (Multiple Endocrine Neoplasia Type 2)
2016, 2017, 2018, 2019
Melanoma
2017
Mitochondrial metabolic disorders
2018, 2019
Molecular testing of germline changes in BRCA genes for ovarian cancer
2017, 2019
Molecular testing of somatic changes in BRCA genes for ovarian cancer
2017, 2018, 2019
MonoDiab (Monogenic Diabetes)
2016, 2017, 2018, 2019
Multiplex oncology pilot EQA
2018
OI (Osteogenesis imperfecta)
2016, 2017, 2018, 2019
ONCOPANEL (Oncogene panel testing) - pilot scheme
2016, 2017, 2018, 2019
PKU (Phenylketonuria)
2016, 2017, 2018, 2019
POR (Porphyria)
2016, 2017, 2018, 2019
PWAS (Prader-Willi and Angelman syndromes)
2016, 2017, 2018, 2019
RB (Retinoblastoma)
2019
RYR1 related disorders
2019
SCA (Spinocerebellar ataxias)
2016, 2017, 2019
SHOX (Short stature homeobox gene testing)
2016, 2017, 2018, 2019
SMA (Spinal muscular atrophy)
2016
VHL (Von Hippel Lindau syndrome)
2017, 2018, 2019
WIL (Wilson disease)
2018, 2019
EQA scheme(s) organized by GenQA
Achondroplasia & Thanatophoric dysplasia
2018
BRCA
2018
BRCA testing for ovarian cancer - somatic
2020, 2021
BRCA testing in ovarian cancer -somatic pilot
2018
Cardiac Disorders
2020
Cardiomyopathies
2018
DNA Quantification
2021
Exome Sequencing Data Interpretation
2021
Fabry disease
2018, 2019
Genetic counselling
2021
Inborn Errors of Metabolism
2020, 2021
Infertility
2020
MCADD Molecular Newborn Screening (bloodspots)
2021
Maternal cell contamination (MCC) & sexing
2019, 2020, 2021
Mismatch repair
2021
NGS somatic pilot
2018
Neurofibromatosis and Rasopathies
2020
Next Generation Sequencing (NGS) germline
2020, 2021
Polyposis (familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP))
2018
Postnatal constitutional Copy Number Variant (CNV) detection
2019, 2020, 2021
Preimplantation Genetic Testing (PGT) for monogenic disorders
2019, 2020, 2021
Respiratory disorders
2021
Rett syndrome
2018
Skeletal dysplasia
2019, 2021
X-inactivation
2019
cfDNA testing in lung cancer pilot
2018
EQA scheme(s) organized by INSTAND
Molekulargenetik SET 08 : DPD exon 14 skipping
2017
Molekulargenetik SET 09 (CFTR)
2017
Molekulargenetik SET 11: Dystrophin
2017
EQA scheme(s) organized by UKNEQAS
Additional lung biomarkers (17-18)
2017
Aortopathies Gene Panel Pilot
2017
Fabry disease
2017
Long QT syndrome
2017
MCADD
2017
MCC & sexing
2017
NIPT for aneuploidies pilot 2017
2017
PGD 2017 Stage 1 CF
2017
PGD 2017 Stage 2 CF
2017
PGD Blastomere/Trophectoderm Array/NGS aneuploidy EQA
2017
PGD Blastomere/Trophectoderm Array/NGS chromosome rearrangement EQA
2017
Dodatkowe informacje
Activities of this institution
Dokumenty zawarte w niniejszej witrynie internetowej są przedstawione wyłącznie w celach informacyjnych. Materiał nie jest w żaden sposób przeznaczony do wymiany profesjonalnej opieki medycznej przez wykwalifikowanego specjalistę i nie powinien być używany jako podstawa do diagnozowania lub leczenia.