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- 2009
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Mark
Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism
(
- Contribution to journal › Article
- 2008
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Mark
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture
(
- Contribution to journal › Article
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Mark
Identifying Genetic Traces of Historical Expansions : Phoenician Footprints in the Mediterranean
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- Contribution to journal › Article
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Mark
Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events
(
- Contribution to journal › Article
- 2007
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Mark
Associating mitochondrial DNA variation with complex traits - Reply to Elson et al.
(
- Contribution to journal › Letter
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Mark
Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities
(
- Contribution to journal › Article
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Mark
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans
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- Contribution to journal › Article
- 2006
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Mark
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration
(
- Contribution to journal › Article
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Mark
Comprehensive association testing of common mitochondrial DNA variation in metabolic disease
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- Contribution to journal › Article
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Mark
Genetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in Sweden.
(
- Contribution to journal › Article