2008 SCHEMES
For the 2008 round of EQA, EMQN will be running the usual schemes as well as four new pilot schemes (for list of schemes see below). The scheme registration opens on 5
th of May and you have until 2
1st July to register to take part in the current years schemes. The cheaper registration period ends in beginning of July (€220.00 per scheme before this date and €250.00 after). For more information, please see the
2008 EQA scheme catalogue.
DISEASE-SPECIFIC EQA SCHEMES Y-chromosome micro deletions (AZF)
Hereditary breast cancer (BRCA)
Congenital Adrenal Hyperplasia (CAH) (
pilot scheme)
Charcot-Marie-Tooth disease (CMT)
Connexin 26 (CNX26) (
pilot scheme)
Myotonic dystrophy (DM)
Duchenne and Becker muscular dystrophies (DMD)
Fragile X syndrome (FRAX)
Friedreich ataxia (FRDA)
Huntington disease (HD)
Hereditary haemochromatosis (HFE)
Hereditary non-polyposis colon cancer (HNPCC)
Monogenic b-cell diabetes (MonoDiab)
Multiple Endocrine Neoplasia Type 2 (MEN2) (
pilot scheme)
Phenylketonuria (PKU)
Porphyria (POR)
Prader-willi and Angelman syndromes (PWAS)
Retinoblastoma (RB)
Spinocerebellar ataxias (SCA)
Spinal muscular atrophy (SMA)
Von Hippel Lindau syndrome (VHL) (
pilot scheme)
Wilson disease (WIL)
TECHNIQUE-SPECIFIC EQA SCHEMES Mutation scanning (MSCAN)
DNA sequencing (SEQ)