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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
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