Andries Westerveld
Affiliations: | University of Amsterdam, Amsterdam, Netherlands |
Area:
human geneticsGoogle:
"Andries Westerveld"Bio:
Prof. dr. A. Westerveld at the Album Academicum of the University of Amsterdam
http://hdl.handle.net/1765/26425
Cross-listing: Chemistry Tree
Parents
Sign in to add mentor| Dirk Bootsma | grad student | 1971 | Erasmus University | |
| (Gene linkage in man and Chinese hamster studied in somatic cell hybrids) | ||||
Children
Sign in to add trainee| Phillip G. de Groot | grad student | 1981 | Amsterdam (Chemistry Tree) |
| Stanley Brul | grad student | 1991 | Amsterdam (Chemistry Tree) |
| Huib N. Caron | grad student | 1995 | Amsterdam (Neurotree) |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Ruigrok YM, Wijmenga C, Rinkel GJ, et al. (2008) Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32. Stroke; a Journal of Cerebral Circulation. 39: 1096-102 |
| Luijten M, Redeker S, Minoshima S, et al. (2001) Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22. Human Genetics. 109: 109-16 |
| Luijten M, Fahsold R, Mischung C, et al. (2001) Limited contribution of interchromosomal gene conversion to NF1 gene mutation. Journal of Medical Genetics. 38: 481-5 |
| Steenman MJ, Zijlstra N, Kruitbosch DL, et al. (2000) Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors. Cytogenetics and Cell Genetics. 88: 289-95 |
| Luijten M, Wang Y, Smith BT, et al. (2000) Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22. European Journal of Human Genetics : Ejhg. 8: 209-14 |
| Alders M, Ryan A, Hodges M, et al. (2000) Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome. American Journal of Human Genetics. 66: 1473-84 |
| van der Drift P, Chan A, Zehetner G, et al. (1999) Multiple MSP pseudogenes in a local repeat cluster on 1p36.2: An expanding genomic graveyard? Genomics. 62: 74-81 |
| Hulsebos TJ, Oskam NT, Bijleveld EH, et al. (1999) Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2. British Journal of Cancer. 81: 1150-4 |
| Steenman M, Tomlinson G, Westerveld A, et al. (1999) Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma. Cytogenetics and Cell Genetics. 86: 157-61 |
| den Hollander AI, ten Brink JB, de Kok YJ, et al. (1999) Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nature Genetics. 23: 217-21 |