Hans van Bokhoven
Affiliations: | Radboudumc |
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| Kleefstra T, Schenck A, Kramer JM, et al. (2014) The genetics of cognitive epigenetics. Neuropharmacology. 80: 83-94 |
| Nillesen WM, Yntema HG, Moscarda M, et al. (2011) Characterization of a novel transcript of the EHMT1 gene reveals important diagnostic implications for Kleefstra syndrome Human Mutation. 32: 853-859 |
| Kleefstra T, Yntema HG, Nillesen WM, et al. (2004) MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics. European Journal of Human Genetics. 12: 24-28 |
| Celli J, Bokhoven Hv, Brunner HG. (2003) Feingold syndrome: clinical review and genetic mapping. American Journal of Medical Genetics Part A. 122: 294-300 |
| Duijf PHG, Bokhoven Hv, Brunner HG. (2003) Pathogenesis of split-hand/split-foot malformation Human Molecular Genetics. 12 |
| Yntema HG, Poppelaars FA, Derksen E, et al. (2002) Expanding phenotype of XNP mutations: mild to moderate mental retardation. American Journal of Medical Genetics. 110: 243-247 |
| Kleefstra T, Yntema HG, Oudakker AR, et al. (2002) Localization of a gene for nonspecific X-linked mental retardation (MRX 76) to Xp22.3-Xp21.3. American Journal of Medical Genetics. 110: 410-411 |
| Yntema HG, Kleefstra T, Oudakker AR, et al. (2002) Low frequency of MECP2 mutations in mentally retarded males. European Journal of Human Genetics. 10: 487-490 |
| Yntema HG, Oudakker AR, Kleefstra T, et al. (2002) In-frame deletion in MECP2 causes mild nonspecific mental retardation American Journal of Medical Genetics. 107: 81-83 |