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1. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

2. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion

3. Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees

4. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1

5. Report of the sixth international workshop on human chromosome 3 mapping 1995

6. A strategy for the prior processing of high-resolution mass spectral data obtained from high-dimensional combined fractional diagonal chromatography.

7. Using a Poisson approximation to predict the isotopic distribution of sulphur-containing peptides in a peptide-centric proteomic approach.

8. Functional analysis of cyclin-dependent kinase inhibitors of Arabidopsis.

9. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

10. Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1.

11. Report of the sixth international workshop on human chromosome 3 mapping 1995.

12. Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.

14. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.

15. On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family.

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