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164 results
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Multiple MSP pseudogenes in a local repeat cluster on 1p36.2: An expanding genomic graveyard?
van der Drift P, Chan A, Zehetner G, Westerveld A, Versteeg R. van der Drift P, et al. Among authors: westerveld a. Genomics. 1999 Nov 15;62(1):74-81. doi: 10.1006/geno.1999.5972. Genomics. 1999. PMID: 10585770
Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2.
Hulsebos TJ, Bijlsma EK, Geurts van Kessel AH, Brakenhoff RH, Westerveld A. Hulsebos TJ, et al. Among authors: westerveld a. Cytogenet Cell Genet. 1991;56(3-4):171-5. doi: 10.1159/000133080. Cytogenet Cell Genet. 1991. PMID: 2055112
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19.
Thompson LH, Bachinski LL, Stallings RL, Dolf G, Weber CA, Westerveld A, Siciliano MJ. Thompson LH, et al. Among authors: westerveld a. Genomics. 1989 Nov;5(4):670-9. doi: 10.1016/0888-7543(89)90107-9. Genomics. 1989. PMID: 2591959
Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22.
Luijten M, Redeker S, Minoshima S, Shimizu N, Westerveld A, Hulsebos TJ. Luijten M, et al. Among authors: westerveld a. Hum Genet. 2001 Jul;109(1):109-16. doi: 10.1007/s004390100543. Hum Genet. 2001. PMID: 11479742
Integrated genetic and physical map of the 1q31-->q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes.
van Soest S, van Rossem MJ, Heckenlively JR, van den Born LI, de Meulemeester TM, Vliex S, de Jong PT, Bleeker-Wagemakers EM, Westerveld A, Bergen AA. van Soest S, et al. Among authors: westerveld a. Cytogenet Cell Genet. 1999;84(1-2):22-7. doi: 10.1159/000015204. Cytogenet Cell Genet. 1999. PMID: 10343093
Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.
Steenman M, Westerveld A, Mannens M. Steenman M, et al. Among authors: westerveld a. Genes Chromosomes Cancer. 2000 May;28(1):1-13. doi: 10.1002/(sici)1098-2264(200005)28:1<1::aid-gcc1>;2-#. Genes Chromosomes Cancer. 2000. PMID: 10738297 Review.
The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.
Alders M, Hodges M, Hadjantonakis AK, Postmus J, van Wijk I, Bliek J, de Meulemeester M, Westerveld A, Guillemot F, Oudejans C, Little P, Mannens M. Alders M, et al. Among authors: westerveld a. Hum Mol Genet. 1997 Jun;6(6):859-67. doi: 10.1093/hmg/6.6.859. Hum Mol Genet. 1997. PMID: 9175731
Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.
Alders M, Bliek J, Redeker B, Ryan A, Feinberg A, Westerveld A, Little P, Mannens M. Alders M, et al. Among authors: westerveld a. Med Pediatr Oncol. 1996 Nov;27(5):495-7. doi: 10.1002/(SICI)1096-911X(199611)27:5<495::AID-MPO18>3.0.CO;2-9. Med Pediatr Oncol. 1996. PMID: 8827080 No abstract available.
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification.
Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voƻte PA, Westerveld A, Versteeg R. Caron H, et al. Among authors: westerveld a. Nat Genet. 1993 Jun;4(2):187-90. doi: 10.1038/ng0693-187. Nat Genet. 1993. PMID: 8102298
Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.
Mannens M, Devilee P, Bliek J, Mandjes I, de Kraker J, Heyting C, Slater RM, Westerveld A. Mannens M, et al. Among authors: westerveld a. Cancer Res. 1990 Jun 1;50(11):3279-83. Cancer Res. 1990. PMID: 2159377
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