Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 162, doi. 10.1111/ahg.12102
- By:
- Publication type:
- Article
Works matching IS 00034800 AND DT 2015 AND VI 79 AND IP 3
Results: 7
1
2
Kullback-Leibler Distance Methods for Detecting Disease Association with Rare Variants from Sequencing Data.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 199, doi. 10.1111/ahg.12103
- By:
- Publication type:
- Article
3
Overlapping Dopaminergic Pathway Genetic Susceptibility to Heroin and Cocaine Addictions in African Americans.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 188, doi. 10.1111/ahg.12104
- By:
- Publication type:
- Article
4
Association of Monocyte Chemoattractant Protein-1 ( MCP-1)-2518A>G Polymorphism with Susceptibility to Coronary Artery Disease: A Meta-Analysis.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 173, doi. 10.1111/ahg.12105
- By:
- Publication type:
- Article
5
Early Myoclonic Encephalopathy in 9q33-q34 Deletion Encompassing STXBP1 and SPTAN1.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 209, doi. 10.1111/ahg.12106
- By:
- Publication type:
- Article
6
A Novel TAZ Gene Mutation and Mosaicism in a Polish Family with Barth Syndrome.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 218, doi. 10.1111/ahg.12108
- By:
- Publication type:
- Article
7
Founder Haplotype Analysis of Fanconi Anemia in the Korean Population Finds Common Ancestral Haplotypes for a FANCG Variant.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 3, p. 153, doi. 10.1111/ahg.12097
- By:
- Publication type:
- Article