β2-Adrenergic Receptor Gene Variations Associated with Stage-2 Hypertension in Northern Han Chinese.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 36, doi. 10.1046/j.1529-8817.2003.00093.x
- By:
- Publication type:
- Article
Works matching IS 00034800 AND DT 2005 AND VI 69 AND IP 1
Results: 13
1
2
Phenotype Severity and Genetic Variation at the Disease Locus: An Investigation of Nail Dysplasia in the Nail Patella Syndrome.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 1, doi. 10.1046/j.1529-8817.2004.00133.x
- By:
- Publication type:
- Article
3
Linkage Analysis of Chromosome 1 with Essential Hypertension and Blood Pressure Quantitative Traits in Chinese Families.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 45, doi. 10.1046/j.1529-8817.2004.00136.x
- By:
- Publication type:
- Article
4
The Contribution of Genetic and Environmental Factors to Quantitative Variability of Erythrocyte Membrane Proteins in Primary Hypotension.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 25, doi. 10.1046/j.1529-8817.2004.00102.x
- By:
- Publication type:
- Article
5
Corrigendum.
- Published in:
- 2005
- Publication type:
- Correction Notice
6
Comprehensive Cystic Fibrosis Mutation Epidemiology and Haplotype Characterization in a Southern Italian Population.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 15, doi. 10.1046/j.1529-8817.2004.00130.x
- By:
- Publication type:
- Article
7
The use of Allelic Expression Differences to Ascertain Functional Polymorphisms Acting incis: Analysis ofMMP1Transcripts in Normal Lung Tissue.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 127, doi. 10.1046/j.1529-8817.2004.00135.x
- By:
- Publication type:
- Article
8
Double Heterozygosity with Mutations Involving both theGJB2andGJB6Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 9, doi. 10.1046/j.1529-8817.2003.00120.x
- By:
- Publication type:
- Article
9
Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 67, doi. 10.1046/j.1529-8817.2003.00127.x
- By:
- Publication type:
- Article
10
Genetic Association Studies in Complex Disease: Disentangling Additional Predisposing Loci from Associated Neutral Loci Using a Constrained - Permutation Approach.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 90, doi. 10.1046/j.1529-8817.2004.00129.x
- By:
- Publication type:
- Article
11
Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 55, doi. 10.1046/j.1529-8817.2004.00138.x
- By:
- Publication type:
- Article
12
Linkage Analysis of Affected Sib Pairs Allowing for Parent-of-Origin Effects.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 113, doi. 10.1046/j.1529-8817.2004.00139.x
- By:
- Publication type:
- Article
13
Fine Mapping Functional Sites or Regions from Case-Control Data Using Haplotypes of Multiple Linked SNPs.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 102, doi. 10.1046/j.1529-8817.2004.00140.x
- By:
- Publication type:
- Article