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- 2014
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Mark
Mitochondrial D-loop and cytochrome oxidase C subunit I polymorphisms among the breast cancer patients of Mizoram, Northeast India
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- Contribution to journal › Article
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Mark
A conserved proline triplet in Val-tRNA synthetase and the origin of elongation factor P
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- Contribution to journal › Article
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Mark
Proteolytic activation of the human epithelial sodium channel by trypsin IV and trypsin I involves distinct cleavage sites
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- Contribution to journal › Article
- 2013
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Mark
Mutation spectrum in South American Lynch syndrome families
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- Contribution to journal › Article
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Mark
Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
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- Contribution to journal › Article
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Mark
Association of estrogen receptor-alpha A908G (K303R) mutation with breast cancer risk
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- Contribution to journal › Article
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Mark
VariBench: A Benchmark Database for Variations
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- Contribution to journal › Article
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Mark
Origin of Swedish hemophilia B mutations
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- Contribution to journal › Article
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Mark
Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders : an overview study
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- Contribution to journal › Article
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Mark
A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual loss
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- Contribution to journal › Article