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N. Hateboer
Institute of Medical Genetics
University Hospital of Wales
Cardiff
UK
Name/email consistency: high
- Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindred. Hateboer, N., Buchalter, M., Davies, S.J., Lazarou, L.P., Ravine, D. Am. J. Kidney Dis. (2000)
- Location of mutations within the PKD2 gene influences clinical outcome. Hateboer, N., Veldhuisen, B., Peters, D., Breuning, M.H., San-Millán, J.L., Bogdanova, N., Coto, E., van Dijk, M.A., Afzal, A.R., Jeffery, S., Saggar-Malik, A.K., Torra, R., Dimitrakov, D., Martinez, I., de Castro, S.S., Krawczak, M., Ravine, D. Kidney Int. (2000)
- Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group. Hateboer, N., v Dijk, M.A., Bogdanova, N., Coto, E., Saggar-Malik, A.K., San Millan, J.L., Torra, R., Breuning, M., Ravine, D. Lancet (1999)
- Familial phenotype differences in PKD11. Hateboer, N., Lazarou, L.P., Williams, A.J., Holmans, P., Ravine, D. Kidney Int. (1999)
