|
Albright hereditary osteodystrophy (AHO), Pseudohypoparathyroidism (PHP)
|
GNAS 20q13.32
|
ME031-GNASbasic research
|
€ 1145€ 572.50
|
|
Beckwith-Wiedemann Syndrome (BWS), Russell-Silver Syndrome (RSS)
|
11p15 region, H19, IGF2, CDKN1C, KCNQ1
|
ME030-BWS/RSS
|
€ 1145
|
|
Fragile X
|
FMR1, AFF2
|
ME029-FMR1/AFF2
|
€ 1145
|
|
Mismatch repair genes (MMR)
|
MLH1, MSH2, MSH6, MLH3, MSH3
|
ME011-MMRimproved
|
€ 1145
|
|
Prader Willi syndrome (PWS), Angelman syndrome (AS)
|
PWS/AS region (15q11-13), MKRN3, MAGEL2, NDN, SNRPN, UBE3A, ATP10A, GABRB3, OCA2
|
ME028-PWS/AS
|
€ 1145
|
|
Repair genes
|
Various
|
ME046-Repairbasic research
|
€ 1145€ 572.50
|
|
Tumour suppressor genes
|
Various
|
ME003-Tumor sup.-3basic research
|
€ 1145
|
|
Tumour suppressor genes
|
Various
|
ME002-Tumor sup.-2basic research
|
€ 1145
|
|
Tumour suppressor genes
|
Various
|
ME001-Tumor sup.-1basic research
|
€ 1145
|
|
Tumour suppressor genes
|
Various
|
ME004-Tumor sup.-4basic research
|
€ 1145
|
|
Tumours, Cutaneous melanoma
|
9p21, CDKN2A, CDKNA2B
|
ME024-9p21
|
€ 1145
|