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Your search keyword '"Wijker M"' showing total 8 results

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1. Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.

2. Evidence for at least eight Fanconi anemia genes.

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3. Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family.

4. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

5. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

6. Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21.

7. Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.

8. The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.