Works matching IS 00034800 AND DT 2013 AND VI 77 AND IP 4
Results: 8
Epistatic Interaction between Genetic Variants in Susceptibility Gene ETS1 Correlates with IL-17 Levels in SLE Patients.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 344, doi. 10.1111/ahg.12018
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- Article
A Novel Mutation in FGD4/FRABIN Causes Charcot Marie Tooth Disease Type 4H in Patients from a Consanguineous Tunisian Family.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 336, doi. 10.1111/ahg.12017
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- Article
A Comparison of the Likelihood Ratio Test and the Variance-Stabilising Transformation-Based Tests for Detecting Association of Rare Variants.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 333, doi. 10.1111/ahg.12022
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- Article
Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 321, doi. 10.1111/ahg.12023
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- Article
The Effect of Genetic Admixture in an Association Study: Genetic Polymorphisms and Chromosome Aberrations in a Colombian Population Exposed to Organic Solvents.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 308, doi. 10.1111/ahg.12019
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- Article
Wilson Disease Mutation Pattern with Genotype-Phenotype Correlations from Western India: Confirmation of p.C271 as a Common Indian Mutation and Identification of 14 Novel Mutations.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 299, doi. 10.1111/ahg.12024
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- Article
The Role of Epistasis in the Etiology of Polycystic Ovary Syndrome among Indian Women: SNP-SNP and SNP-Environment Interactions.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 288, doi. 10.1111/ahg.12020
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- Article
Genome-Wide Association Study of Pre-Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy-Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort.
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- Annals of Human Genetics, 2013, v. 77, n. 4, p. 277, doi. 10.1111/ahg.12021
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- Article