Works matching IS 00034800 AND DT 2014 AND VI 78 AND IP 1
Results: 7
Dominant PRPF31 Mutations Are Hypostatic to a Recessive CNOT3 Polymorphism in Retinitis Pigmentosa: A Novel Phenomenon of 'Linked Trans-Acting Epistasis'.
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- Annals of Human Genetics, 2014, v. 78, n. 1, p. 62, doi. 10.1111/ahg.12042
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- Article
The Dopamine Receptor D2 ( DRD2) SNP rs1076560 is Associated with Opioid Addiction.
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- Annals of Human Genetics, 2014, v. 78, n. 1, p. 33, doi. 10.1111/ahg.12046
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- Article
Genetic Evaluation and Application of Posterior Cranial Fossa Traits as Endophenotypes for Chiari Type I Malformation.
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- Annals of Human Genetics, 2014, v. 78, n. 1, p. 1, doi. 10.1111/ahg.12041
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- Article
A Novel GBA2 Gene Missense Mutation in Spastic Ataxia.
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- Annals of Human Genetics, 2014, v. 78, n. 1, p. 13, doi. 10.1111/ahg.12045
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- Article
Genetic Variation in the Peroxisome Proliferator-Activated Receptor (PPAR) and Peroxisome Proliferator-Activated Receptor Gamma Co-activator 1 (PGC1) Gene Families and Type 2 Diabetes.
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- Annals of Human Genetics, 2014, v. 78, n. 1, p. 23, doi. 10.1111/ahg.12044
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- Article
Comparing the Efficacy of SNP Filtering Methods for Identifying a Single Causal SNP in a Known Association Region.
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- Annals of Human Genetics, 2014, v. 78, n. 1, p. 50, doi. 10.1111/ahg.12043
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- Article
Heritability of Phenotypes Associated with Glucose Homeostasis and Adiposity in a Rural Area of Brazil.
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- Annals of Human Genetics, 2014, v. 78, n. 1, p. 40, doi. 10.1111/ahg.12047
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- Article