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Results:
1-17
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Results: 17
Authors:
van den Berg, JSP
Limburg, M
Pals, G
Arwert, F
Westerveld, A
Citation: Jsp. Van Den Berg et al., Type III collagen deficiency in a family with intracranial aneurysms, CEREB DIS, 11(2), 2001, pp. 92-94
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:
Luijten, M
Redeker, S
Minoshima, S
Shimizu, N
Westerveld, A
Hulsebos, TJM
Citation: M. Luijten et al., Duplication and transposition of the NF1 pseudogene regions on chromosomes2, 14, and 22, HUM GENET, 109(1), 2001, pp. 109-116
Authors:
Ratsma, JE
van der Stelt, O
Schoffelmeer, ANM
Westerveld, A
Gunning, WB
Citation: Je. Ratsma et al., P3 event-related potential, dopamine D2 receptor A1 allele, and sensation-seeking in adult children of alcoholics, ALC CLIN EX, 25(7), 2001, pp. 960-967
Authors:
Luijten, M
Fahsold, R
Mischung, C
Westerveld, A
Nurnberg, P
Hulsebos, TJM
Citation: M. Luijten et al., Limited contribution of interchromosomal gene conversion to NF1 gene mutation, J MED GENET, 38(7), 2001, pp. 481-484
Authors:
Steenman, M
Westerveld, A
Mannens, M
Citation: M. Steenman et al., Genetics of Beckwith-Wiedemann syndrome-associated tumors: Common genetic pathways, GENE CHROM, 28(1), 2000, pp. 1-13
Authors:
Luijten, M
Wang, YP
Smith, BT
Westerveld, A
Smink, LJ
Dunham, I
Roe, BA
Hulsebos, TJM
Citation: M. Luijten et al., Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22, EUR J HUM G, 8(3), 2000, pp. 209-214
Authors:
Luijten, M
Redeker, S
van Noesel, MM
Troost, D
Westerveld, A
Hulsebos, TJM
Citation: M. Luijten et al., Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas, EUR J HUM G, 8(12), 2000, pp. 939-945
Authors:
Steenman, MJC
Zijlstra, N
Kruitbosch, DL
Wiesmeijer, C
Larizza, L
Voute, PA
Westerveld, A
Mannens, MMAM
Citation: Mjc. Steenman et al., Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors, CYTOG C GEN, 88(3-4), 2000, pp. 289-295
Authors:
Alders, M
Ryan, A
Hodges, M
Bliek, J
Feinberg, AP
Privitera, O
Westerveld, A
Little, PFR
Mannens, M
Citation: M. Alders et al., Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome, AM J HU GEN, 66(5), 2000, pp. 1473-1484
Authors:
den Hollander, AI
ten Brink, JB
de Kok, YJM
van Soest, S
van den Born, LI
van Driel, MA
van de Pol, DJR
Payne, AM
Bhattacharya, SS
Kellner, U
Hoyng, CB
Westerveld, A
Brunner, HG
Bleeker-Wagemakers, EM
Deutman, AF
Heckenlively, JR
Cremers, FPM
Bergen, AAB
Citation: Ai. Den Hollander et al., Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12), NAT GENET, 23(2), 1999, pp. 217-221
Authors:
van der Drift, P
Chan, A
Zehetner, G
Westerveld, A
Versteeg, R
Citation: P. Van Der Drift et al., Multiple MSP pseudogenes in a local repeat cluster on 1p36.2: An expandinggenomic graveyard?, GENOMICS, 62(1), 1999, pp. 74-81
Authors:
Steenman, M
Tomlinson, G
Westerveld, A
Mannens, M
Citation: M. Steenman et al., Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma, CYTOG C GEN, 86(2), 1999, pp. 157-161
Authors:
van Soest, S
van Rossem, MJ
Heckenlively, JR
van den Born, LI
de Meulemeester, TMAMO
Vliex, S
de Jong, PTVM
Bleeker-Wagemakers, EM
Westerveld, A
Bergen, AAB
Citation: S. Van Soest et al., Integrated genetic and physical map of the 1q3 -> q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes, CYTOG C GEN, 84(1-2), 1999, pp. 22-27
Authors:
Van Soest, S
Westerveld, A
De Jong, PTVM
Bleeker-Wagemakers, EM
Bergen, AAB
Citation: S. Van Soest et al., Retinitis pigmentosa: Defined from a molecular point of view, SURV OPHTHA, 43(4), 1999, pp. 321-334
Authors:
van den Berg, JSP
Pals, G
Arwert, F
Hennekam, RCM
Albrecht, KW
Westerveld, A
Limburg, M
Citation: Jsp. Van Den Berg et al., Type III collagen deficiency in saccular intracranial aneurysms - Defect in gene regulation?, STROKE, 30(8), 1999, pp. 1628-1631
Authors:
Hulsebos, TJM
Oskam, NT
Bijleveld, EH
Westerveld, A
Hermsen, MA
van den Ouweland, AMW
Hamel, BC
Tijssen, CC
Citation: Tjm. Hulsebos et al., Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2, BR J CANC, 81(7), 1999, pp. 1150-1154
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1-17
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