A. Westerveld

发表

High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.

P F Little, D J Porteous, D. Porteous, 1992, Genomics.

The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.

F. Guillemot, P. Little, A. Hadjantonakis, 1997, Human molecular genetics.

Chromosome 11 Putative Tumor Suppressor Regions , Is Limited to Loss of Heterozygosity in Wilms ' Tumors , Studied for Six Updated

C. Heyting, P. Devilee, A. Westerveld, 2006 .

The chromosomal localization of human β-galactosidase revisited: a locus for β-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22

H. J. Sips, H. Galjaard, A. Westerveld, 2004, Human Genetics.

Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma

M. Mannens, A. Westerveld, Marja Steenman, 1999, Cytogenetic and Genome Research.

The distal region of 11p13 and associated genetic diseases.

C. Junien, G. Saunders, B. Williams, 1991, Genomics.

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.

L. Sandkuijl, A. Bergen, A. Westerveld, 1994, Genomics.

A human modifier of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1.

F. Speleman, R. Versteeg, A. Westerveld, 1996, Human molecular genetics.

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

P. D. de Jong, J. Heckenlively, A. Bergen, 1999, Cytogenetic and Genome Research.

Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.

A. Westerveld, M. Alders, M. Mannens, 1995, Cytogenetics and cell genetics.

Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.

F. Speleman, R. Versteeg, N. Van Roy, 1995, Oncogene.

Limited contribution of interchromosomal gene conversion toNF1 gene mutation

C. Mischung, T. Hulsebos, Andries Westerveld, 2001, Journal of medical genetics.

Differences between rodent and human cell lines in the amount of integrated DNA after transfection.

J. Hoeijmakers, A. Westerveld, H. Odijk, 1987, Experimental cell research.

Genome-Wide Linkage in a Large Dutch Consanguineous Family Maps a Locus for Intracranial Aneurysms to Chromosome 2p13

M. Limburg, G. Pals, M. Vermeulen, 2004, Stroke.

Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.

C. Heyting, A. Westerveld, M. Mannens, 1989, Cytogenetics and cell genetics.

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.

R. Wanders, R. Schutgens, H. Heymans, 1988, The Journal of clinical investigation.

Multiple MSP pseudogenes in a local repeat cluster on 1p36.2: An expanding genomic graveyard?

G. Zehetner, R. Versteeg, A. Westerveld, 1999, Genomics.