Authors:
Bliek, J
Maas, SM
Ruijter, JM
Hennekam, RCM
Alders, M
Westerveld, A
Mannens, MMAM
Citation: J. Bliek et al., Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS, HUM MOL GEN, 10(5), 2001, pp. 467-476
Authors:
Hofstra, RMW
Wu, Y
Stulp, RP
Elfferich, P
Osinga, J
Maas, SM
Siderius, L
Brooks, AS
Von der Ende, JJ
Heydendael, VMR
Severijnen, RSVM
Bax, KMA
Meijers, C
Buys, CHCM
Citation: Rmw. Hofstra et al., RET and GDNF gene scanning in Hirschprung patients using two dual denaturing gel systems, HUM MUTAT, 15(5), 2000, pp. 418-429
Authors:
Maas, SM
Hoovers, JMN
van Seggelen, ME
Menzel, DM
Hennekam, RCM
Citation: Sm. Maas et al., Interstitial deletion of the long arm of chromosome 2: a clinically recognizable microdeletion syndrome?, CLIN DYSMOR, 9(1), 2000, pp. 47-53
Authors:
Maas, SM
van Engeland, M
Leeksma, NG
Bleichrodt, RP
Citation: Sm. Maas et al., A modification of the "components separation" technique for closure of abdominal wall defects in the presence of an enterostorny, J AM COLL S, 189(1), 1999, pp. 138-140