Orphanet: MVZ PD Dr. Volkmann und Kollegen
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MVZ PD Dr. Volkmann und Kollegen

  • Labor PD Dr. Volkmann und Kollegen
  • Kriegsstr. 99
  • 76133 KARLSRUHE
  • GERMANY
  • Status : -
  • Phone : 49 (0)721 85000152
  • Additional Phone : -
  • Fax : 49 (0)721 85000115
  • Website
  • Contact
  • EUGT number : EUGTDE140235

Contacts

Quality management

EQA
 EQA

EQA scheme(s) organized by CF Network

CF (Cystic fibrosis)
2015, 2016, 2017, 2018, 2019

EQA scheme(s) organized by EMQN

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, 2018, 2019
DFNB1 (Hereditary Deafness)
2017, 2018, 2019
DM (Myotonic dystrophy)
2016, 2017, 2018, 2019
DMD (Duchenne and Becker muscular dystrophies)
2016, 2017, 2018, 2019
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, 2017, 2018, 2019
FRDA (Friedreich ataxia)
2016, 2017, 2018, 2019
Germline NGS mutation testing
2016, 2017, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2016, 2017, 2018, 2019
HD (Huntington disease)
2016, 2017, 2018, 2019
HNPCC (Hereditary non-polyposis colon cancer)
2016, 2017, 2018, 2019
HRF (Hereditary Recurrent Fevers)
2016, 2017, 2018, 2019
MEN2 (Multiple Endocrine Neoplasia Type 2)
2016, 2017, 2018, 2019
Molecular testing of germline changes in BRCA genes for ovarian cancer
2017, 2018
Molecular testing of somatic changes in BRCA genes for ovarian cancer
2017, 2018
MonoDiab (Monogenic Diabetes)
2016, 2017, 2018, 2019
PKU (Phenylketonuria)
2017, 2018, 2019
POR (Porphyria)
2016, 2017, 2018, 2019
PWAS (Prader-Willi and Angelman syndromes)
2016, 2017, 2018, 2019
RYR1 related disorders
2019
SCA (Spinocerebellar ataxias)
2016, 2017, 2018, 2019
SHOX (Short stature homeobox gene testing)
2016, 2017, 2018, 2019
SMA (Spinal muscular atrophy)
2016, 2017, 2018, 2019
Somatic NGS mutation testing
2016, 2017
VHL (Von Hippel Lindau syndrome)
2016, 2017, 2018, 2019
WIL (Wilson disease)
2016, 2017, 2018, 2019

EQA scheme(s) organized by GenQA

cfDNA testing in lung cancer pilot
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.