Works matching IS 00034800 AND DT 2012 AND VI 76 AND IP 4
Results: 7
Novel Mutation in Potassium Channel related Gene KCTD7 and Progressive Myoclonic Epilepsy.
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- Annals of Human Genetics, 2012, v. 76, n. 4, p. 326, doi. 10.1111/j.1469-1809.2012.00710.x
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- Article
Bayes Factor Based on the Trend Test Incorporating Hardy-Weinberg Disequilibrium: More Power to Detect Genetic Association.
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- Annals of Human Genetics, 2012, v. 76, n. 4, p. 301, doi. 10.1111/j.1469-1809.2012.00714.x
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- Article
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy.
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- Annals of Human Genetics, 2012, v. 76, n. 4, p. 277, doi. 10.1111/j.1469-1809.2012.00713.x
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Apolipoprotein E/C1/C4/C2 Gene Cluster Diversity in Two Native Andean Populations: Aymaras and Quechuas.
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- Annals of Human Genetics, 2012, v. 76, n. 4, p. 283, doi. 10.1111/j.1469-1809.2012.00712.x
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- Article
The Joint Association of REST and NFKB1 Polymorphisms on the Risk of Colorectal Cancer.
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- Annals of Human Genetics, 2012, v. 76, n. 4, p. 269, doi. 10.1111/j.1469-1809.2012.00709.x
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- Article
Familial Clustering Strongly Suggests that the Phenotypic Variation of the 8344 A>G Lys Mitochondrial tRNA Mutation is Encoded in cis.
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- Annals of Human Genetics, 2012, v. 76, n. 4, p. 296, doi. 10.1111/j.1469-1809.2012.00711.x
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- Article
A Unified Framework for Haplotype Inference in Nuclear Families.
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- Annals of Human Genetics, 2012, v. 76, n. 4, p. 312, doi. 10.1111/j.1469-1809.2012.00715.x
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- Article