11 results on '"Kamino, Kouzin"'
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2. Genetic deficiency of a mitochondrial aldehyde dehydrogenase increases serum lipid peroxides in community-dwelling females
3. Linkage and haplotype analysis of familial early-onset Alzheimer disease in Japanese population
4. Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus
5. Evidence against DNA polymerase β as a candidate gene for Werner syndrome
6. Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2–p22
7. Aphidicolin-resistant human cell lines resistant to uv and bleomycin
8. Dinucleotide repeat polymorphism at the D8S1055
9. Two dinucleotide repeat polymorphisms at the D8S1442 and D8S1443 loci
10. Identification of a single base polymorphism in intron 2 of the c-fos gene and its detection by mismatched PCR-RFLP
11. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers
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