Authors:
VERHOEF S
VRTEL R
BAKKER L
STOLTEDIJKSTRA I
NELLIST M
BEGEER JH
ZAREMBA J
JOZWIAK S
TEMPELAARS AMP
LINDHOUT D
HALLEY DJJ
VANDENOUWELAND AMW
Citation: S. Verhoef et al., RECURRENT MUTATION 4882DELTT IN THE GAP-RELATED DOMAIN OF THE TUBEROUS SCLEROSIS TSC2 GENE, Human mutation, 1998, pp. 85-87
Authors:
VANZELDERENBHOLA SL
BRESLAUSIDERIUS EJ
BEVERSTOCK GC
STOLTEDIJKSTRA I
DEVRIES LS
DEPATER JM
Citation: Sl. Vanzelderenbhola et al., PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION T(17-20) (P13.3-Q13.3) DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION, Prenatal diagnosis, 17(2), 1997, pp. 173-179
Authors:
VERSCHUURENBEMELMANS CC
BRUNT ERP
BURTON M
MENSINK RGJ
VANDERMEULEN MA
SMIT NH
STOLTEDIJKSTRA I
BUYS CHCM
SCHEFFER H
Citation: Cc. Verschuurenbemelmans et al., REFINEMENT BY LINKAGE ANALYSIS IN 2 LARGE FAMILIES OF THE CANDIDATE REGION OF THE 3RD LOCUS (SCA3) FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIATYPE-I, Human genetics, 96(6), 1995, pp. 691-694
Authors:
DEVRIES BBA
ROBINSON H
STOLTEDIJKSTRA I
GI CVTP
DIJKSTRA PF
VANDOOM J
HALLEY DJJ
OOSTRA BA
TURNER G
NIERMEIJER MF
Citation: Bba. Devries et al., GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION, Journal of Medical Genetics, 32(10), 1995, pp. 764-769